Canonical Allele Identifier: PA102895
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 286014
ClinVar RCV Id: RCV000494055 RCV001385137 RCV000675176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Ala600Thr
CA10605332
NM_005476.7:c.1798G>A