Canonical Allele Identifier: PA2830122171
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2574163
ClinVar RCV Id: RCV003318528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met382Thr
CA367398764
NM_033507.3:c.1145T>C