Allele Registry

Canonical Allele Identifier: PA261261

Gene: DLD HGNC NCBI

ClinVar Allele:

48685

ClinVar RCV:

RCV000033218

ClinVar Variation:

40188

HGVS (amino-acid)	Matching Registered Transcripts
NP_000099.2:p.Ile47Thr	CA261260 NM_000108.5:c.140T>C