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Mutations on the Protein: P10916 From Positions: 50 To 58

3
2
0
1



Swiss-Prot Disease: VAR_004604
p.ARG58GLN
N/A
N/A
Cardiomyopathy, familial hypertrophic 10 (CMH10)


Swiss-Prot Polymorphism: VAR_029449
p.GLY57ARG
N/A
N/A
N/A


OMIM Disease: 160781.0004
p.ARG58GLN
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10






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