Allele Registry

Canonical Allele Identifier: PA2579977057

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000419860

ClinVar Variation:

381599

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Met235Val	CA16605219 NM_000162.5:c.703A>G