Canonical Allele Identifier: PA2825669256
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2265405
ClinVar RCV Id: RCV002808835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Gln418Lys
CA363512272
NM_001128590.3:c.1252C>A