Canonical Allele Identifier: PA120732
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9829
ClinVar RCV Id: RCV000010503 RCV000582333 RCV000814875 RCV001269861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Arg309His
CA120731
NM_001011645.3:c.926G>A