Canonical Allele Identifier: PA120722
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9823
ClinVar RCV Id: RCV000010497 RCV000532628 RCV000582251 RCV003982834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Arg856His
CA120721
NM_000044.6:c.2567G>A