Canonical Allele Identifier: PA2830123260
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1447652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu183Pro
CA367401589
NM_033508.3:c.548T>C