Canonical Allele Identifier: PA2826157822
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 498627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Ser594Phe
CA373424635
NM_001190383.3:c.1781C>T