Canonical Allele Identifier: PA2826157958
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 837972
ClinVar RCV Id: RCV001039420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Leu130Phe
CA5056711
NM_001190384.3:c.388C>T