Allele Registry

Canonical Allele Identifier: PA2830123368

Gene: GCK HGNC NCBI

ClinVar Allele:

1246257

ClinVar RCV:

RCV001663670

ClinVar Variation:

1256328

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Asn203Asp	CA367401360 NM_033508.3:c.607A>G