Canonical Allele Identifier: PA2826767583
Gene: DLD HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276680.1:p.Ile370Thr
CA256135
NM_001289751.1:c.1109T>C