Canonical Allele Identifier: PA2827937310
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233996
ClinVar RCV Id: RCV004527572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Gly30Cys
CA367398311
NM_001354802.1:c.88G>T