Canonical Allele Identifier: PA2825669185
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3079400
ClinVar RCV Id: RCV004367794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Ala274Gly
CA363507424
NM_001128590.3:c.821C>G