Allele Registry

Canonical Allele Identifier: PA120697

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010484

ClinVar Variation:

9810

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Tyr764Cys	CA120695 NM_000044.6:c.2291A>G