Allele Registry

Canonical Allele Identifier: PA2827937247

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003993704

ClinVar Variation:

3068512

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341730.1:p.Ala117Val	CA367396861 NM_001354801.1:c.350C>T