Canonical Allele Identifier: PA2828286132
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 193595
ClinVar RCV Id: RCV000173700 RCV000987670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355073.1:p.Arg301Cys
CA239136
NM_001368144.1:c.901C>T