Canonical Allele Identifier: PA2579979616
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972806
ClinVar RCV Id: RCV001249060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly193Arg
CA4239599
NM_000162.5:c.577G>C
CA367401514
NM_000162.5:c.577G>A