Allele Registry

Canonical Allele Identifier: PA213845

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029916

RCV002463609

RCV002472938

ClinVar Variation:

36253

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Val253Gly	CA213844 NM_000162.5:c.758T>G