Canonical Allele Identifier: PA2827202996
Gene: DIS3L HGNC NCBI

Linked Data

ClinVar Variation Id: 161529
ClinVar RCV Id: RCV000149064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310872.1:p.Gly660Glu
CA174272
NM_001323943.1:c.1979G>A