Canonical Allele Identifier: PA916017249
Gene: DLD HGNC NCBI
ClinVar RCV:
RCV000185848
ClinVar Variation:
203674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276681.1:p.Ala61Val
CA312451
NM_001289752.1:c.182C>T