Allele Registry

Canonical Allele Identifier: PA645461066

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029845

RCV000493278

RCV001248970

ClinVar Variation:

36182

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Ala388Val	CA213727 NM_033507.3:c.1163C>T