Allele Registry

Canonical Allele Identifier: PA2827937357

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003993704

ClinVar Variation:

3068512

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341731.1:p.Ala74Val	CA367396861 NM_001354802.1:c.221C>T