Canonical Allele Identifier: PA2826767751
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 2151483
ClinVar RCV Id: RCV003061361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276681.1:p.Lys229Asn
CA368857275
NM_001289752.1:c.687G>C
CA368857277
NM_001289752.1:c.687G>T