Canonical Allele Identifier: PA256138
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 11971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000099.2:p.Glu375Lys
CA256137
NM_000108.5:c.1123G>A