Allele Registry

Canonical Allele Identifier: PA2827937438

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003993704

ClinVar Variation:

3068512

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341732.1:p.Ala132Val	CA367396861 NM_001354803.2:c.395C>T