Canonical Allele Identifier: PA2828286009
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1264327
ClinVar RCV Id: RCV001667853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355072.1:p.Gly290Val
CA363511936
NM_001368143.1:c.869G>T