Canonical Allele Identifier: PA2828550498
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_001361726.1:p.Leu457Ser
CA16041312
NM_001374797.1:c.1370T>C