Canonical Allele Identifier: PA2580229376
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807286
ClinVar RCV Id: RCV002475243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Lys92Asn
CA367398236
NM_001354803.2:c.276G>T
CA367398238
NM_001354803.2:c.276G>C