Allele Registry

Canonical Allele Identifier: PA2830123479

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000419860

ClinVar Variation:

381599

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Met234Val	CA16605219 NM_033508.3:c.700A>G