Allele Registry

Canonical Allele Identifier: PA658669156

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000516995

RCV004527383

ClinVar Variation:

447389

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Phe424Ser	CA367397256 NM_033507.3:c.1271T>C