Canonical Allele Identifier: PA1139684504
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 854942
ClinVar RCV Id: RCV001060093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Cys88Tyr
CA413429329
NM_001011645.3:c.263G>A