Canonical Allele Identifier: PA2827937264
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Cys2Arg
CA367398754
NM_001354802.1:c.4T>C