Allele Registry

Canonical Allele Identifier: PA2827936673

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000017521

RCV000190348

RCV001281107

RCV003318493

ClinVar Variation:

16141

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Met210Lys	CA204367 NM_001354800.1:c.629T>A