Allele Registry

Canonical Allele Identifier: PA120770

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010516

RCV000584561

ClinVar Variation:

9842

492796

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Met249Ile	CA120769 NM_001011645.3:c.747G>T CA413426471 NM_001011645.3:c.747G>A CA413426473 NM_001011645.3:c.747G>C