Canonical Allele Identifier: PA658804159
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 499322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121699.1:p.Ala667Val
CA5056396
NM_001128227.3:c.2000C>T