Canonical Allele Identifier: PA2830122086
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801683
ClinVar RCV Id: RCV002463842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ser376Thr
CA367398856
NM_033507.3:c.1126T>A