Allele Registry

Canonical Allele Identifier: PA096418

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000992058

RCV003117664

RCV003493767

ClinVar Variation:

804852

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Met210Thr	CA367401300 NM_000162.5:c.629T>C