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Mutations on the Protein: P37231 From Positions: 177 To 202

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OMIM Disease: 601487.0015
p.ARG194TRP
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3


OMIM Disease: 601487.0014
p.CYS190SER
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3






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