Allele Registry

Canonical Allele Identifier: PA2830123818

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003397220

ClinVar Variation:

2628365

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Ala377Pro	CA367398808 NM_033508.3:c.1129G>C