Canonical Allele Identifier: PA239808
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 194025
ClinVar RCV Id: RCV000277092 RCV000315879 RCV000372863 RCV000430334 RCV000545813 RCV003416070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121699.1:p.Val727Leu
CA239806
NM_001128227.3:c.2179G>T
CA373424372
NM_001128227.3:c.2179G>C