Allele Registry

Canonical Allele Identifier: PA2827936661

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV002227423

ClinVar Variation:

1679544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Asp205Val	CA367401343 NM_001354800.1:c.614A>T