Canonical Allele Identifier: PA2826767627
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 40186
ClinVar RCV Id: RCV000033216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276680.1:p.Asp456Val
CA261256
NM_001289751.1:c.1367A>T