Canonical Allele Identifier: PA2826157959
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 283114
ClinVar RCV Id: RCV000266878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Leu131Phe
CA10604401
NM_001190384.3:c.391C>T