Allele Registry

Canonical Allele Identifier: PA120707

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010488

ClinVar Variation:

9814

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Met256Val	CA120706 NM_001011645.3:c.766A>G