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Mutations on the Protein: NP_001011645 From Positions: 39 To 58

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OMIM Disease: 313700.0035
p.CYS47PHE
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0051
p.GLY45ARG
N/A
N/A
ANDROGEN INSENSITIVITY SYNDROME


OMIM Disease: 313700.0007
p.LYS56TER
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0036
p.PHE50TYR
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE






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