Allele Registry

Canonical Allele Identifier: PA120693

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010483

ClinVar Variation:

9809

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Ser116Asn	CA120692 NM_001011645.3:c.347G>A