Allele Registry

Canonical Allele Identifier: PA2830122485

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV001776634

RCV003313230

RCV003401708

ClinVar Variation:

1320655

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Ser442Trp	CA367397017 NM_033507.3:c.1325C>G