Allele Registry

Canonical Allele Identifier: PA916039375

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000479890

RCV002431386

RCV003493592

ClinVar Variation:

418228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341732.1:p.Asp41Asn	CA16618466 NM_001354803.2:c.121G>A