Allele Registry

Canonical Allele Identifier: PA916039402

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029848

RCV002463595

RCV003330312

ClinVar Variation:

36185

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341732.1:p.Arg70Leu	CA213733 NM_001354803.2:c.209G>T