Canonical Allele Identifier: PA2741868023
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Gly64Asp
CA367396980
NM_001354802.1:c.191G>A