Canonical Allele Identifier: PA2826158621
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 283278
ClinVar RCV Id: RCV000484722 RCV000596066 RCV000707707 RCV001165685 RCV004021128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Asp319Tyr
CA5056560
NM_001190388.2:c.955G>T