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Mutations on the Protein: P50461 From Positions: 49 To 58

3
0
0
3


OMIM Disease: 600824.0002
p.CYS58GLY
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12


OMIM Disease: 600824.0004
p.GLU55GLY
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12


OMIM Disease: 600824.0004
p.SER54ARG
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12






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