Canonical Allele Identifier: PA256136
Gene: DLD HGNC NCBI
ClinVar RCV:
RCV000012747
ClinVar Variation:
11969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000099.2:p.Ile393Thr
CA256135
NM_000108.5:c.1178T>C