Allele Registry

Canonical Allele Identifier: PA2827936648

Gene: GCK HGNC NCBI

ClinVar Allele:

195211

ClinVar RCV:

RCV000711778

RCV002272161

RCV002354464

RCV003883139

ClinVar Variation:

198050

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Ala201Ser	CA246541 NM_001354800.1:c.601G>T