Canonical Allele Identifier: PA2826158734
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 370826
ClinVar RCV Id: RCV000411466 RCV001861380 RCV003480623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Leu449Ser
CA16041312
NM_001190388.2:c.1346T>C