Canonical Allele Identifier: PA2829588821
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1377441
ClinVar RCV Id: RCV001912236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Ala522Ser
CA373426301
NM_005476.7:c.1564G>T