Canonical Allele Identifier: PA2827202615
Gene: DIS3L HGNC NCBI

Linked Data

ClinVar Variation Id: 161529
ClinVar RCV Id: RCV000149064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310865.1:p.Gly947Glu
CA174272
NM_001323936.2:c.2840G>A