Canonical Allele Identifier: PA2579979018
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 546098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ile225Met
CA367401129
NM_000162.5:c.675C>G