Canonical Allele Identifier: PA102032
Gene: DLD HGNC NCBI
ClinVar RCV:
RCV000012746
ClinVar Variation:
11968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000099.2:p.Arg495Gly
CA256134
NM_000108.5:c.1483A>G