Canonical Allele Identifier: PA2829588630
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 499709
ClinVar RCV Id: RCV000594865 RCV000673098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Tyr434Cys
CA373427973
NM_005476.7:c.1301A>G