Allele Registry

Canonical Allele Identifier: PA213728

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029845

RCV000493278

RCV001248970

ClinVar Variation:

36182

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Ala387Val	CA213727 NM_000162.5:c.1160C>T