Allele Registry

Canonical Allele Identifier: PA2827936637

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000992056

ClinVar Variation:

804850

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Arg191Gly	CA367401531 NM_001354800.1:c.571C>G