Allele Registry

Canonical Allele Identifier: PA2830123394

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000992058

RCV003117664

RCV003493767

ClinVar Variation:

804852

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Met209Thr	CA367401300 NM_033508.3:c.626T>C