Canonical Allele Identifier: PA916039410
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Phe97Leu
CA367397305
NM_001354803.2:c.291C>G
CA367397306
NM_001354803.2:c.291C>A
CA367397316
NM_001354803.2:c.289T>C