Canonical Allele Identifier: PA2826767297
Gene: DLD HGNC NCBI
ClinVar RCV:
RCV000012747
ClinVar Variation:
11969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276679.1:p.Ile294Thr
CA256135
NM_001289750.1:c.881T>C