Allele Registry

Canonical Allele Identifier: PA2827936644

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003887333

ClinVar Variation:

3026940

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Asp198Ala	CA367401419 NM_001354800.1:c.593A>C