Canonical Allele Identifier: PA2830123304
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972806
ClinVar RCV Id: RCV001249060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly192Arg
CA4239599
NM_033508.3:c.574G>C
CA367401514
NM_033508.3:c.574G>A