Canonical Allele Identifier: PA2573296727
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1678597
ClinVar RCV Id: RCV002225198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met252Val
CA367400634
NM_033507.3:c.754A>G