Canonical Allele Identifier: PA2826767873
Gene: DLD HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276681.1:p.Arg447Gly
CA256134
NM_001289752.1:c.1339A>G