Canonical Allele Identifier: PA2573235098
Gene: CAD HGNC NCBI

Linked Data

ClinVar Variation Id: 1445864
ClinVar RCV Id: RCV001992687 RCV002563452
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004332.2:p.Arg842His
CA1573039
NM_004341.4:c.2525G>A