Canonical Allele Identifier: PA2826157729
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 581094
ClinVar RCV Id: RCV000704818 RCV001167797 RCV001167796 RCV001726313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Gly473Cys
CA373425910
NM_001190383.3:c.1417G>T