Canonical Allele Identifier: PA2573097842
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1314557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Trp168Gly
CA367401767
NM_033507.3:c.502T>G