Allele Registry

Canonical Allele Identifier: PA2825042409

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003327892

ClinVar Variation:

2579457

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Asp205His	CA367401349 NM_000162.5:c.613G>C