Allele Registry

Canonical Allele Identifier: PA2827936655

Gene: GCK HGNC NCBI

ClinVar Allele:

1246257

ClinVar RCV:

RCV001663670

ClinVar Variation:

1256328

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Asn204Asp	CA367401360 NM_001354800.1:c.610A>G