Allele Registry

Canonical Allele Identifier: PA2830123372

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV002227423

ClinVar Variation:

1679544

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Asp204Val	CA367401343 NM_033508.3:c.611A>T