Canonical Allele Identifier: PA1139748803
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe153Leu
CA367401920
NM_033507.3:c.459T>G
CA367401922
NM_033507.3:c.459T>A
CA367401929
NM_033507.3:c.457T>C