Mutations on the Protein: P50461 From Positions: 39 To 49
Swiss-Prot Disease: VAR_045932 
p.LEU44PRO
N/A
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N/A
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Cardiomyopathy, familial hypertrophic 12 (CMH12)
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OMIM Disease: 600824.0003 
p.LEU44PRO
N/A
| |
N/A
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CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12
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|---|
OMIM Disease: 600824.0006 
p.SER46ARG
N/A
| |
N/A
|
|---|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12
|
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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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