Canonical Allele Identifier: PA2826158700
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 598714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Val411Leu
CA5056495
NM_001190388.2:c.1231G>C
CA373427085
NM_001190388.2:c.1231G>T