Mutations on the Protein: P22309 From Positions: 480 To 506
Swiss-Prot Disease: VAR_007709 
p.TYR486ASP
N/A
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N/A
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Transient familial neonatal hyperbilirubinemia (HBLRTFN)
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OMIM Disease: 191740.0017 
p.TYR486ASP
N/A
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N/A
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HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATAL||CRIGLER-NAJJAR SYNDROME, TYPE II, INCLUDED
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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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