Canonical Allele Identifier: PA2826767548
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 1966956
ClinVar RCV Id: RCV002721682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276680.1:p.Leu299Phe
CA368857692
NM_001289751.1:c.897G>C
CA368857693
NM_001289751.1:c.897G>T