Allele Registry

Canonical Allele Identifier: PA2830123558

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000518148

RCV002413397

RCV003325962

ClinVar Variation:

447417

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Ala258Val	CA367400579 NM_033508.3:c.773C>T