Canonical Allele Identifier: PA2826157750
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Val498Leu
CA274932
NM_001190383.3:c.1492G>C
CA373425687
NM_001190383.3:c.1492G>T