Canonical Allele Identifier: PA2828549754
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 496947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361726.1:p.Cys13Ser
CA373422109
NM_001374797.1:c.38G>C
CA373422116
NM_001374797.1:c.37T>A