Canonical Allele Identifier: PA2827427155
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Ala597Thr
CA120703
NM_001348061.1:c.1789G>A