Canonical Allele Identifier: PA2827936429
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1299600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Glu48Lys
CA4239714
NM_001354800.1:c.142G>A