Canonical Allele Identifier: PA645451451
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 280062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Asn772His
CA10603629
NM_000044.6:c.2314A>C