Canonical Allele Identifier: PA102061
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 11965
ClinVar RCV Id: RCV000012743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000099.2:p.Pro488Leu
CA256133
NM_000108.5:c.1463C>T