Canonical Allele Identifier: PA2828551421
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361727.1:p.Ala401Val
CA253707
NM_001374798.1:c.1202C>T