Canonical Allele Identifier: PA2827936959
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233999
ClinVar RCV Id: RCV004527575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu386Arg
CA367398699
NM_001354800.1:c.1157T>G