Canonical Allele Identifier: PA2830123807
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801683
ClinVar RCV Id: RCV002463842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ser374Thr
CA367398856
NM_033508.3:c.1120T>A