Allele Registry

Canonical Allele Identifier: PA120762

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010513

ClinVar Variation:

9839

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Phe51Tyr	CA120761 NM_001011645.3:c.152T>A