Canonical Allele Identifier: PA2827937113
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg40His
CA213715
NM_001354801.1:c.119G>A