Canonical Allele Identifier: PA2830123808
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2767216
ClinVar RCV Id: RCV003573794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ser374Tyr
CA367398843
NM_033508.3:c.1121C>A