Canonical Allele Identifier: PA2830123754
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 908615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr341Pro
CA157913750
NM_033508.3:c.1021A>C