Allele Registry

Canonical Allele Identifier: PA916039351

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000516995

RCV004527383

ClinVar Variation:

447389

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341730.1:p.Phe86Ser	CA367397256 NM_001354801.1:c.257T>C