Allele Registry

Canonical Allele Identifier: PA120708

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010488

ClinVar Variation:

9814

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Met788Val	CA120706 NM_000044.6:c.2362A>G