Canonical Allele Identifier: PA253690
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Val622Met
CA253688
NM_001190383.3:c.1864G>A