Canonical Allele Identifier: PA2827936588
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1309623
ClinVar RCV Id: RCV001765792
ClinVar Variation Id: 1685845
ClinVar RCV Id: RCV002250012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Trp167Cys
CA367401757
NM_001354800.1:c.501G>T
CA367401759
NM_001354800.1:c.501G>C