Allele Registry

Canonical Allele Identifier: PA120719

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010496

ClinVar Variation:

9822

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Val335Leu	CA120718 NM_001011645.3:c.1003G>T CA413428104 NM_001011645.3:c.1003G>C