Canonical Allele Identifier: PA2826157501
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1714136
ClinVar RCV Id: RCV002297119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Ser199Arg
CA373417996
NM_001190383.3:c.597C>G
CA373417997
NM_001190383.3:c.597C>A
CA373418003
NM_001190383.3:c.595A>C