Allele Registry

Canonical Allele Identifier: PA2579982938

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000518148

RCV002413397

RCV003325962

ClinVar Variation:

447417

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Ala259Val	CA367400579 NM_000162.5:c.776C>T