Allele Registry

Canonical Allele Identifier: PA120794

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010535

ClinVar Variation:

9860

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Ser741Cys	CA120792 NM_000044.6:c.2222C>G