Canonical Allele Identifier: PA2827937109
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801683
ClinVar RCV Id: RCV002463842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ser38Thr
CA367398856
NM_001354801.1:c.112T>A