Allele Registry

Canonical Allele Identifier: PA645460248

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000419860

ClinVar Variation:

381599

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Met236Val	CA16605219 NM_033507.3:c.706A>G