Allele Registry

Canonical Allele Identifier: PA916050250

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000992058

RCV003117664

RCV003493767

ClinVar Variation:

804852

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Met211Thr	CA367401300 NM_033507.3:c.632T>C