Canonical Allele Identifier: PA2827936705
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly227Ser
CA367401117
NM_001354800.1:c.679G>A