Canonical Allele Identifier: PA2825669166
Gene: CYP21A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 242688
ClinVar RCV Id: RCV001269964 RCV002250603 RCV002298552
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122062.3:p.Met210Lys
CA358446
NM_001128590.3:c.629T>A