Allele Registry

Canonical Allele Identifier: PA120702

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010478

RCV001056795

RCV001818149

ClinVar Variation:

9804

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Arg775Cys	CA120701 NM_000044.6:c.2323C>T