Allele Registry

Canonical Allele Identifier: PA120739

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010505

ClinVar Variation:

9831

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Thr878Ala	CA120737 NM_000044.6:c.2632A>G