Canonical Allele Identifier: PA2580303532
Gene: CAD HGNC NCBI

Linked Data

ClinVar Variation Id: 2164820
ClinVar RCV Id: RCV003088229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004332.2:p.Arg842Cys
CA346211555
NM_004341.4:c.2524C>T