Canonical Allele Identifier: PA2826158783
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2923716
ClinVar RCV Id: RCV003783274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Ser501Arg
CA373425773
NM_001190388.2:c.1503C>G
CA373425775
NM_001190388.2:c.1503C>A
CA373425785
NM_001190388.2:c.1501A>C