Allele Registry

Canonical Allele Identifier: PA2830124087

Gene: GCK HGNC NCBI

ClinVar Allele:

3227839

ClinVar RCV:

RCV003993704

ClinVar Variation:

3068512

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Ala453Val	CA367396861 NM_033508.3:c.1358C>T