Allele Registry

Canonical Allele Identifier: PA120790

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010533

ClinVar Variation:

9858

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Gly212Glu	CA120789 NM_001011645.3:c.635G>A