Canonical Allele Identifier: PA2741997491
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2574157
ClinVar RCV Id: RCV003318522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr169Ala
CA367401753
NM_033507.3:c.505A>G