Allele Registry

Canonical Allele Identifier: PA120775

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010520

RCV000224621

RCV001519068

RCV002247311

RCV003234899

RCV003982835

ClinVar Variation:

9846

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Gln267Glu	CA120774 NM_001011645.3:c.799C>G