Canonical Allele Identifier: PA916029822
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 492780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334993.1:p.Ala385Ser
CA10436391
NM_001348064.1:c.1153G>T