Canonical Allele Identifier: PA2826158840
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Ala572Val
CA253717
NM_001190388.2:c.1715C>T