Canonical Allele Identifier: PA2827936811
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Glu279Lys
CA157915593
NM_001354800.1:c.835G>A