Canonical Allele Identifier: PA658716091
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 492780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Ala385Ser
CA10436391
NM_000044.6:c.1153G>T