Allele Registry

Canonical Allele Identifier: PA2825042404

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV004545931

ClinVar Variation:

3234078

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Asn204Lys	CA367401352 NM_000162.5:c.612T>G CA367401354 NM_000162.5:c.612T>A