Canonical Allele Identifier: PA1139668261
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 995351
ClinVar RCV Id: RCV001289400 RCV003416152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Arg409His
CA363511663
NM_000500.9:c.1226G>A