Canonical Allele Identifier: PA120797
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Ala646Asp
CA120795
NM_000044.6:c.1937C>A