Allele Registry

Canonical Allele Identifier: PA254901

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010526

ClinVar Variation:

9852

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Leu181Phe	CA254900 NM_001011645.3:c.541C>T