Canonical Allele Identifier: PA2826158785
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2952697
ClinVar RCV Id: RCV003817831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Phe503Val
CA373425761
NM_001190388.2:c.1507T>G