Canonical Allele Identifier: PA2828550473
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2416741
ClinVar RCV Id: RCV003108992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361726.1:p.Gln442His
CA5056476
NM_001374797.1:c.1326A>C
CA373426695
NM_001374797.1:c.1326A>T