Allele Registry

Canonical Allele Identifier: PA2830122678

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000445500

RCV000992041

ClinVar Variation:

393454

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Met40Thr	CA16609270 NM_033508.3:c.119T>C