Canonical Allele Identifier: PA2826157367
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 496947
ClinVar RCV Id: RCV000594728 RCV000755013 RCV001853994
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Cys13Ser
CA373422109
NM_001190383.3:c.38G>C
CA373422116
NM_001190383.3:c.37T>A