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Mutations on the Protein: NP_001011645 From Positions: 252 To 272

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OMIM Disease: 313700.0043
p.GLN266GLU
N/A
N/A
ANDROGEN INSENSITIVITY, PARTIAL


OMIM Disease: 313700.0012
p.MET254VAL
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE


OMIM Disease: 313700.0006
p.TRP262TER
N/A
N/A
ANDROGEN INSENSITIVITY, COMPLETE






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