Allele Registry

Canonical Allele Identifier: PA120696

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010484

ClinVar Variation:

9810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Tyr232Cys	CA120695 NM_001011645.3:c.695A>G