Canonical Allele Identifier: PA2827937369
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233999
ClinVar RCV Id: RCV004527575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Leu64Arg
CA367398699
NM_001354803.2:c.191T>G