Canonical Allele Identifier: PA2826157880
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 290713
ClinVar RCV Id: RCV000400388 RCV000534256 RCV000657912 RCV003323497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Arg12Trp
CA10606885
NM_001190384.3:c.34A>T