Canonical Allele Identifier: PA2827936805
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val277Gly
CA367400467
NM_001354800.1:c.830T>G