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Mutations on the Protein: P63316 From Positions: 145 To 153

2
1
0
1






Swiss-Prot Disease: VAR_063073
p.ASP145GLU
N/A
N/A
Cardiomyopathy, familial hypertrophic 13 (CMH13)


OMIM Disease: 191040.0005
p.ASP145GLU
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13






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