Allele Registry

Canonical Allele Identifier: PA120756

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010511

ClinVar Variation:

9837

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Leu176Arg	CA120755 NM_001011645.3:c.527T>G