Canonical Allele Identifier: PA2825669187
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1809584
ClinVar RCV Id: RCV002481158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Val276Gly
CA363507470
NM_001128590.3:c.827T>G