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Mutations on the Protein: NP_733822 From Positions: 32 To 63

3
0
0
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OMIM Disease: 150330.0030
p.ALA57PRO
N/A
N/A
CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTRIPIC HYPOGONADISM


OMIM Disease: 150330.0005
p.ARG60GLY
N/A
N/A
CARDIOMYOPATHY, DILATED, 1A||LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2, INCLUDED


OMIM Disease: 150330.0052
p.LEU59ARG
N/A
N/A
CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTRIPIC HYPOGONADISM






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