Canonical Allele Identifier: PA2826158471
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1714136
ClinVar RCV Id: RCV002297119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Ser140Arg
CA373417996
NM_001190388.2:c.420C>G
CA373417997
NM_001190388.2:c.420C>A
CA373418003
NM_001190388.2:c.418A>C