Canonical Allele Identifier: PA2830123545
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 994610
ClinVar RCV Id: RCV001288181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Trp256Ser
CA367400594
NM_033508.3:c.767G>C