Canonical Allele Identifier: PA915957785
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 800634
ClinVar RCV Id: RCV000984612
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000491.4:p.Met261Thr
CA363506205
NM_000500.9:c.782T>C