Mutations on the Protein: P68133 From Positions: 0 To 19
Swiss-Prot Disease: VAR_062424 
p.ASP3TYR
N/A
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N/A
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Nemaline myopathy 3 (NEM3)
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Swiss-Prot Disease: VAR_011680 
p.GLY17ARG
N/A
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N/A
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Myopathy, actin, congenital, with excess of thin myofilaments (MPCETM)
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OMIM Disease: 102610.0003 
p.GLY15ARG
N/A
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N/A
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MYOPATHY, ACTIN, CONGENITAL, WITH EXCESS OF THIN MYOFILAMENTS
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: 
Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.
| DMDM_info@umbc.edu | 1000 Hilltop Circle, Baltimore, MD
21250 | Department of Biological Sciences | Phone: 410-455-2258 |
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3
2
0
1