Canonical Allele Identifier: PA2580303552
Gene: CAD HGNC NCBI

Linked Data

ClinVar Variation Id: 2010613
ClinVar RCV Id: RCV002834116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004332.2:p.Ala877Ser
CA346212121
NM_004341.4:c.2629G>T