Canonical Allele Identifier: PA312467
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 203681
ClinVar RCV Id: RCV000676803 RCV000653827 RCV001161965 RCV001161966 RCV004020251 RCV004545876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000099.2:p.Arg263His
CA312466
NM_000108.5:c.788G>A