Canonical Allele Identifier: PA2830122260
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2169517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg395Pro
CA367398581
NM_033507.3:c.1184G>C
CA2695203000
NM_033507.3:c.1184_1185delinsCG