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Mutations on the Protein: Q01955 From Positions: 1086 To 1169

2
1
0
1



Swiss-Prot Disease: VAR_011211
p.GLY1167ARG
N/A
N/A
Alport syndrome, autosomal dominant (APSAD)


OMIM Disease: 120070.0010
p.GLY1167ARG
N/A
N/A
ALPORT SYNDROME, AUTOSOMAL DOMINANT






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