Allele Registry

Canonical Allele Identifier: PA645461101

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000445420

RCV001584122

RCV004539920

ClinVar Variation:

393447

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Ala455Glu	CA16609264 NM_033507.3:c.1364C>A