Canonical Allele Identifier: PA2827936986
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2578359
ClinVar RCV Id: RCV003326085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg397Gly
CA367398536
NM_001354800.1:c.1189C>G