Canonical Allele Identifier: PA2829587942
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 496947
ClinVar RCV Id: RCV000594728 RCV000755013 RCV001853994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Cys13Ser
CA373422109
NM_005476.7:c.38G>C
CA373422116
NM_005476.7:c.37T>A