Canonical Allele Identifier: PA2825669182
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 800594
ClinVar RCV Id: RCV000984572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Ala256Ser
CA363506991
NM_001128590.3:c.766G>T