Canonical Allele Identifier: PA2580303498
Gene: CAD HGNC NCBI

Linked Data

ClinVar Variation Id: 2125232
ClinVar RCV Id: RCV003040011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004332.2:p.Thr804Ala
CA346211163
NM_004341.4:c.2410A>G