Canonical Allele Identifier: PA2825669180
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2136374
ClinVar RCV Id: RCV003037144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.His253Asn
CA363506898
NM_001128590.3:c.757C>A