Allele Registry

Canonical Allele Identifier: PA2830123774

Gene: GCK HGNC NCBI

ClinVar Variation Id: 418228

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Asp362Asn	CA16618466 NM_033508.3:c.1084G>A