Canonical Allele Identifier: PA2828285999
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 800598
ClinVar RCV Id: RCV000984576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355072.1:p.Arg266Gly
CA363511394
NM_001368143.1:c.796A>G