Canonical Allele Identifier: PA916029817
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 804018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334993.1:p.Ser176Arg
CA10436287
NM_001348064.1:c.528C>A
CA413425066
NM_001348064.1:c.526A>C
CA413425072
NM_001348064.1:c.528C>G