Allele Registry

Canonical Allele Identifier: PA645460208

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000017521

RCV000190348

RCV001281107

RCV003318493

ClinVar Variation:

16141

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Met211Lys	CA204367 NM_033507.3:c.632T>A