Canonical Allele Identifier: PA2827936639
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972806
ClinVar RCV Id: RCV001249060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly193Arg
CA4239599
NM_001354800.1:c.577G>C
CA367401514
NM_001354800.1:c.577G>A