Canonical Allele Identifier: PA645460254
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg251His
CA4239531
NM_033507.3:c.752G>A