Canonical Allele Identifier: PA915956339
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 434266
ClinVar RCV Id: RCV000499725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Arg84Cys
CA413429305
NM_001011645.3:c.250C>T