Canonical Allele Identifier: PA2827936562
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1741488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Phe152Ser
CA367401925
NM_001354800.1:c.455T>C