Canonical Allele Identifier: PA2580229372
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801514
ClinVar RCV Id: RCV002463834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Gly88Val
CA367398308
NM_001354803.2:c.263G>T