Canonical Allele Identifier: PA2825026763
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 1685535
ClinVar RCV Id: RCV002249262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Trp399Arg
CA10436397
NM_000044.6:c.1195T>C
CA413426583
NM_000044.6:c.1195T>A