Allele Registry

Canonical Allele Identifier: PA120757

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010511

ClinVar Variation:

9837

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Leu708Arg	CA120755 NM_000044.6:c.2123T>G