Allele Registry

Canonical Allele Identifier: PA645460196

Gene: GCK HGNC NCBI

ClinVar Allele:

195211

ClinVar RCV:

RCV000711778

RCV002272161

RCV002354464

RCV003883139

ClinVar Variation:

198050

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Ala202Ser	CA246541 NM_033507.3:c.604G>T