Canonical Allele Identifier: PA645451357
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 268093
ClinVar RCV Id: RCV000258807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Ile562Thr
CA10602648
NM_000044.6:c.1685T>C