Allele Registry

Canonical Allele Identifier: PA2827936672

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000992058

RCV003117664

RCV003493767

ClinVar Variation:

804852

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Met210Thr	CA367401300 NM_001354800.1:c.629T>C