Canonical Allele Identifier: PA2827936699
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 546098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ile225Met
CA367401129
NM_001354800.1:c.675C>G