Allele Registry

Canonical Allele Identifier: PA2827936664

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000117132

RCV000497903

RCV001844042

RCV003343641

ClinVar Variation:

129145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Thr206Pro	CA152955 NM_001354800.1:c.616A>C