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Mutations on the Protein: P08100 From Positions: 278 To 296

2
1
0
1





Swiss-Prot Disease: VAR_004827
p.ALA292GLU
N/A
N/A
Night blindness, congenital stationary, autosomal dominant 1 (CSNBAD1)


OMIM Disease: 180380.0031
p.ALA292GLU
N/A
N/A
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1






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