Canonical Allele Identifier: PA2828551478
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 424619
ClinVar RCV Id: RCV000487445 RCV000763619 RCV003139687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361727.1:p.Ala465Val
CA5056466
NM_001374798.1:c.1394C>T