Allele Registry

Canonical Allele Identifier: PA2830123370

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV004545931

ClinVar Variation:

3234078

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Asn203Lys	CA367401352 NM_033508.3:c.609T>G CA367401354 NM_033508.3:c.609T>A