Allele Registry

Canonical Allele Identifier: PA2579979477

Gene: GCK HGNC NCBI

ClinVar Variation Id: 2503893

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Gly44Cys	CA367403443 NM_000162.5:c.130G>T