Allele Registry

Canonical Allele Identifier: PA645460340

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029827

RCV002463591

ClinVar Variation:

36164

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Phe335_Val336delinsLeuMet	CA213696 NM_033507.3:c.1005_1006delinsAA