Canonical Allele Identifier: PA261257
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 40186
ClinVar RCV Id: RCV000033216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000099.2:p.Asp479Val
CA261256
NM_000108.5:c.1436A>T