Canonical Allele Identifier: PA2826158897
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 194025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Val637Leu
CA239806
NM_001190388.2:c.1909G>T
CA373424372
NM_001190388.2:c.1909G>C