Canonical Allele Identifier: PA2827937328
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.His36Arg
CA367398216
NM_001354802.1:c.107A>G