Canonical Allele Identifier: PA2826158318
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 498627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Ser558Phe
CA373424635
NM_001190384.3:c.1673C>T