Allele Registry

Canonical Allele Identifier: PA120738

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010505

ClinVar Variation:

9831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Thr346Ala	CA120737 NM_001011645.3:c.1036A>G