Canonical Allele Identifier: PA891849541
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 585748
ClinVar RCV Id: RCV000711369
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Arg427Cys
CA363511962
NM_000500.9:c.1279C>T