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Mutations on the Protein: NP_001011645 From Positions: 349 To 369

2
0
0
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OMIM Disease: 313700.0009
p.LYS350TER
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0048
p.SER356SER
N/A
N/A
ANDROGEN INSENSITIVITY SYNDROME






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