Canonical Allele Identifier: PA2827936694
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136520
ClinVar RCV Id: RCV003060105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly223Val
CA367401157
NM_001354800.1:c.668G>T