Canonical Allele Identifier: PA102888
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_005467.1:p.Ala524Val
CA5056466
NM_005476.7:c.1571C>T