Canonical Allele Identifier: PA2826767782
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 1966956
ClinVar RCV Id: RCV002721682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276681.1:p.Leu274Phe
CA368857692
NM_001289752.1:c.822G>C
CA368857693
NM_001289752.1:c.822G>T