Canonical Allele Identifier: PA2827936951
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995100
ClinVar RCV Id: RCV001288973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala384Pro
CA367398729
NM_001354800.1:c.1150G>C