Canonical Allele Identifier: PA2827937059
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly444Asp
CA367396980
NM_001354800.1:c.1331G>A