Canonical Allele Identifier: PA916029832
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334993.1:p.Arg569His
CA120703
NM_001348064.1:c.1706G>A