Allele Registry

Canonical Allele Identifier: PA2579981023

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000479890

RCV002431386

RCV003493592

ClinVar Variation:

418228

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Asp363Asn	CA16618466 NM_000162.5:c.1087G>A