Canonical Allele Identifier: PA1139748653
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg37Gln
CA367403564
NM_033507.3:c.110G>A