Canonical Allele Identifier: PA120762
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9839
ClinVar RCV Id: RCV000010513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Phe51Tyr
CA120761
NM_001011645.3:c.152T>A