Canonical Allele Identifier: PA2830123528
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 450262
ClinVar Variation Id: 1045215
ClinVar RCV Id: RCV001349584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asn253Lys
CA367400610
NM_033508.3:c.759T>G
CA367400611
NM_033508.3:c.759T>A