Canonical Allele Identifier: PA1139749084
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 994610
ClinVar RCV Id: RCV001288181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Trp258Ser
CA367400594
NM_033507.3:c.773G>C