Canonical Allele Identifier: PA2828286005
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3030523
ClinVar RCV Id: RCV003901722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355072.1:p.Arg274Leu
CA363511665
NM_001368143.1:c.821G>T