Allele Registry

Canonical Allele Identifier: PA645461108

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000017520

RCV002513079

ClinVar Variation:

16140

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Val456Met	CA257432 NM_033507.3:c.1366G>A