Canonical Allele Identifier: PA2827936453
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly68Asp
CA157919943
NM_001354800.1:c.203G>A