Canonical Allele Identifier: PA2579982450
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 429500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg447Gln
CA367396940
NM_000162.5:c.1340G>A