Allele Registry

Canonical Allele Identifier: PA096438

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000017518

RCV002513078

RCV003147297

RCV003147298

RCV003147299

ClinVar Variation:

16138

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Ser131Pro	CA126213 NM_000162.5:c.391T>C