Canonical Allele Identifier: PA2830123760
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu354Pro
CA367399180
NM_033508.3:c.1061T>C