Canonical Allele Identifier: PA120787
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9857
ClinVar RCV Id: RCV000010531 RCV000010532 RCV001851781
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Gly212Val
CA120786
NM_001011645.3:c.635G>T