Allele Registry

Canonical Allele Identifier: PA261259

Gene: DLD HGNC NCBI

ClinVar RCV:

RCV000033217

ClinVar Variation:

40187

HGVS (amino-acid)	Matching Registered Transcripts
NP_000099.2:p.Arg482Gly	CA261258 NM_000108.5:c.1444A>G