Allele Registry

Canonical Allele Identifier: PA120754

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010510

RCV001305872

ClinVar Variation:

9836

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Ala722Thr	CA120752 NM_000044.6:c.2164G>A