Canonical Allele Identifier: PA120697
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9810
ClinVar RCV Id: RCV000010484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Tyr764Cys
CA120695
NM_000044.6:c.2291A>G