Canonical Allele Identifier: PA2580150885
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1702701
ClinVar RCV Id: RCV002279019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121699.1:p.Trp544Leu
CA373426404
NM_001128227.3:c.1631G>T