Allele Registry

Canonical Allele Identifier: PA120787

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010531

RCV000010532

RCV001851781

ClinVar Variation:

9857

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Gly212Val	CA120786 NM_001011645.3:c.635G>T