Canonical Allele Identifier: PA2573181580
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1451631
ClinVar RCV Id: RCV002035345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.His39Leu
CA363499053
NM_001128590.3:c.116A>T