Allele Registry

Canonical Allele Identifier: PA213718

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029840

RCV001642240

RCV002444444

RCV003318495

ClinVar Variation:

36177

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Ala379Glu	CA213717 NM_000162.5:c.1136C>A