Canonical Allele Identifier: PA916026961
Gene: DIS3L HGNC NCBI

Linked Data

ClinVar Variation Id: 161529
ClinVar RCV Id: RCV000149064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310877.1:p.Gly970Glu
CA174272
NM_001323948.2:c.2909G>A