Allele Registry

Canonical Allele Identifier: PA645459510

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029872

RCV000255585

RCV001248967

RCV001253600

RCV002426523

RCV003546683

ClinVar Variation:

36209

976334

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Gly73Arg	CA213771 NM_033507.3:c.217G>A CA367403112 NM_033507.3:c.217G>C