Allele Registry

Canonical Allele Identifier: PA2827936722

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000419860

ClinVar Variation:

381599

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Met235Val	CA16605219 NM_001354800.1:c.703A>G