Canonical Allele Identifier: PA2826767409
Gene: DLD HGNC NCBI
ClinVar RCV:
RCV003093606
ClinVar Variation:
2158694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276680.1:p.Tyr54Phe
CA4434372
NM_001289751.1:c.161A>T