Canonical Allele Identifier: PA2828550565
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 424619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361726.1:p.Ala473Val
CA5056466
NM_001374797.1:c.1418C>T