Canonical Allele Identifier: PA2827936706
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2580859
ClinVar RCV Id: RCV003330054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly227Arg
CA367401116
NM_001354800.1:c.679G>C