Allele Registry

Canonical Allele Identifier: PA645461111

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000017525

RCV001818166

ClinVar Variation:

16143

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Ala457Val	CA257433 NM_033507.3:c.1370C>T