Canonical Allele Identifier: PA2826157882
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1420269
ClinVar RCV Id: RCV001914149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Ile16_Val17delinsMet
CA588147230
NM_001190384.3:c.48_50del