Canonical Allele Identifier: PA2827937110
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2767216
ClinVar RCV Id: RCV003573794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ser38Tyr
CA367398843
NM_001354801.1:c.113C>A