Canonical Allele Identifier: PA2828285942
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 804728
ClinVar RCV Id: RCV000991866 RCV001805959 RCV002488087
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355072.1:p.Pro133Leu
CA3732545
NM_001368143.1:c.398C>T