Canonical Allele Identifier: PA916050096
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 76898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly45Ser
CA157920006
NM_033507.3:c.133G>A