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Mutations on the Protein: NP_001011645 From Positions: 233 To 252

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OMIM Disease: 313700.0011
p.ALA239THR
N/A
N/A
ANDROGEN INSENSITIVITY, PARTIAL


OMIM Disease: 313700.0010
p.ARG240CYS
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0003
p.ARG241CYS
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0015
p.ARG241HIS
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0039
p.MET248ILE
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE






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