Canonical Allele Identifier: PA2580229365
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2121221
ClinVar RCV Id: RCV003049053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Val79Ile
CA4239414
NM_001354803.2:c.235G>A