Allele Registry

Canonical Allele Identifier: PA2830123886

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029845

RCV000493278

RCV001248970

ClinVar Variation:

36182

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Ala386Val	CA213727 NM_033508.3:c.1157C>T