Allele Registry

Canonical Allele Identifier: PA915956342

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000489065

ClinVar Variation:

427107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Arg98Trp	CA413422950 NM_001011645.3:c.292C>T