Canonical Allele Identifier: PA2830123567
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 211075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asp261Asn
CA206279
NM_033508.3:c.781G>A