Canonical Allele Identifier: PA2826907783
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_001293008.1:p.Thr741Ala
CA346211163
NM_001306079.2:c.2221A>G