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Mutations on the Protein: P10916 From Positions: 91 To 100

2
1
0
1


Swiss-Prot Disease: VAR_004605
p.PRO95ALA
N/A
N/A
Cardiomyopathy, familial hypertrophic 10 (CMH10)


OMIM Disease: 160781.0003
p.PRO94ARG
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10






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