Canonical Allele Identifier: PA2826158794
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Val513Leu
CA274932
NM_001190388.2:c.1537G>C
CA373425687
NM_001190388.2:c.1537G>T