Canonical Allele Identifier: PA2741823913
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 3062281
ClinVar RCV Id: RCV003986003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Met93Val
CA413429362
NM_001011645.3:c.277A>G