Allele Registry

Canonical Allele Identifier: PA2827936562

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV002340196

RCV004527446

ClinVar Variation:

1741488

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Phe152Ser	CA367401925 NM_001354800.1:c.455T>C