Canonical Allele Identifier: PA658804122
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 496947
ClinVar RCV Id: RCV000594728 RCV000755013 RCV001853994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121699.1:p.Cys44Ser
CA373422109
NM_001128227.3:c.131G>C
CA373422116
NM_001128227.3:c.130T>A