Canonical Allele Identifier: PA2580124523
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1807431
ClinVar RCV Id: RCV002475388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.His403Arg
CA3732668
NM_000500.9:c.1208A>G