Canonical Allele Identifier: PA2828550490
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 499667
ClinVar RCV Id: RCV000591966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361726.1:p.Leu453Phe
CA5056473
NM_001374797.1:c.1357C>T