Canonical Allele Identifier: PA2828551123
Gene: GNE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361727.1:p.Met112Val
CA253719
NM_001374798.1:c.334A>G