Canonical Allele Identifier: PA2829589218
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_005467.1:p.Ser668Phe
CA373424635
NM_005476.7:c.2003C>T