Canonical Allele Identifier: PA2826767348
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 11965
ClinVar RCV Id: RCV000012743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276679.1:p.Pro389Leu
CA256133
NM_001289750.1:c.1166C>T