Canonical Allele Identifier: PA645459526
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129143
ClinVar Variation Id: 3024423
ClinVar RCV Id: RCV003883459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly176Arg
CA231137
NM_033507.3:c.526G>A
CA367401686
NM_033507.3:c.526G>C