Canonical Allele Identifier: PA312465
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 203680
ClinVar RCV Id: RCV000185855 RCV000298315 RCV000408335 RCV001086796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000099.2:p.Met255Leu
CA312464
NM_000108.5:c.763A>C
CA164257674
NM_000108.5:c.763A>T