Canonical Allele Identifier: PA102041
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 11966
ClinVar RCV Id: RCV000012744 RCV000185853 RCV000624277 RCV004528103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000099.2:p.Gly229Cys
CA312461
NM_000108.5:c.685G>T