Canonical Allele Identifier: PA2826767352
Gene: DLD HGNC NCBI
ClinVar RCV:
RCV000012746
ClinVar Variation:
11968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276679.1:p.Arg396Gly
CA256134
NM_001289750.1:c.1186A>G