Canonical Allele Identifier: PA2830123195
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_277043.1:p.Trp166Cys
CA367401757
NM_033508.3:c.498G>T
CA367401759
NM_033508.3:c.498G>C