Allele Registry

Canonical Allele Identifier: PA096238

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000194319

RCV000880473

RCV003313054

RCV003335189

RCV003992227

ClinVar Variation:

211076

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Glu279Gln	CA208420 NM_000162.5:c.835G>C