Canonical Allele Identifier: PA658804161
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 498627
ClinVar RCV Id: RCV000593521 RCV001854024 RCV003459467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121699.1:p.Ser699Phe
CA373424635
NM_001128227.3:c.2096C>T