Canonical Allele Identifier: PA2828286002
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1675319
ClinVar RCV Id: RCV002211048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355072.1:p.Phe270Ser
CA363511482
NM_001368143.1:c.809T>C