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Mutations on the Protein: P63316 From Positions: 24 To 32

3
1
0
2





Swiss-Prot Disease: VAR_019776
p.LEU29GLN
N/A
N/A
Cardiomyopathy, familial hypertrophic 13 (CMH13)


OMIM Disease: 191040.0006
p.ALA31SER
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13


OMIM Disease: 191040.0002
p.LEU29GLN
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13






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