Canonical Allele Identifier: PA916047142
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12150
ClinVar RCV Id: RCV000622562 RCV000711382 RCV003226157 RCV000012933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355073.1:p.Ile38Asn
CA341179
NM_001368144.1:c.113T>A