Allele Registry

Canonical Allele Identifier: PA120729

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010502

ClinVar Variation:

9828

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Arg609Lys	CA120728 NM_000044.6:c.1826G>A