Canonical Allele Identifier: PA2826907808
Gene: CAD HGNC NCBI

Linked Data

ClinVar Variation Id: 1524147
ClinVar RCV Id: RCV002049076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293008.1:p.Ile781Asn
CA1573040
NM_001306079.2:c.2342T>A