Canonical Allele Identifier: PA2830123894
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ile389Thr
CA213731
NM_033508.3:c.1166T>C