Canonical Allele Identifier: PA2826767341
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 40186
ClinVar RCV Id: RCV000033216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276679.1:p.Asp380Val
CA261256
NM_001289750.1:c.1139A>T