Canonical Allele Identifier: PA2827427120
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 268093
ClinVar RCV Id: RCV000258807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Ile562Thr
CA10602648
NM_001348061.1:c.1685T>C