Canonical Allele Identifier: PA2826158762
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2429378
ClinVar RCV Id: RCV003126315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Phe478Leu
CA373426097
NM_001190388.2:c.1434T>G
CA373426099
NM_001190388.2:c.1434T>A
CA373426107
NM_001190388.2:c.1432T>C