Canonical Allele Identifier: PA2827937422
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Gly122Asp
CA367396980
NM_001354803.2:c.365G>A