Canonical Allele Identifier: PA2825202150
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1675316
ClinVar RCV Id: RCV002211045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Arg125Cys
CA3732374
NM_000500.9:c.373C>T