Canonical Allele Identifier: PA2830123052
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asp131Asn
CA4239636
NM_033508.3:c.391G>A