Allele Registry

Canonical Allele Identifier: PA2579976942

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000445500

RCV000992041

ClinVar Variation:

393454

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Met41Thr	CA16609270 NM_000162.5:c.122T>C