Allele Registry

Canonical Allele Identifier: PA2580490804

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003037218

ClinVar Variation:

2136522

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Asp206Tyr	CA367401348 NM_033507.3:c.616G>T