Canonical Allele Identifier: PA120776
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Gln799Glu
CA120774
NM_000044.6:c.2395C>G