Canonical Allele Identifier: PA2580229369
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807287
ClinVar RCV Id: RCV002475244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Gly85Asp
CA367398350
NM_001354803.2:c.254G>A