Allele Registry

Canonical Allele Identifier: PA645459501

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000445500

RCV000992041

ClinVar Variation:

393454

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Met42Thr	CA16609270 NM_033507.3:c.125T>C