Canonical Allele Identifier: PA2827937329
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2571660
ClinVar RCV Id: RCV003313370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Phe39Val
CA367397313
NM_001354802.1:c.115T>G