Canonical Allele Identifier: PA2826767866
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 40187
ClinVar RCV Id: RCV000033217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276681.1:p.Arg434Gly
CA261258
NM_001289752.1:c.1300A>G