Canonical Allele Identifier: PA120796
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Ala114Asp
CA120795
NM_001011645.3:c.341C>A