Canonical Allele Identifier: PA2830123143
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2628364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg154Ser
CA367401896
NM_033508.3:c.462G>T
CA367401898
NM_033508.3:c.462G>C