Allele Registry

Canonical Allele Identifier: PA645460361

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000479890

RCV002431386

RCV003493592

ClinVar Variation:

418228

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Asp364Asn	CA16618466 NM_033507.3:c.1090G>A