Canonical Allele Identifier: PA2830122203
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995100
ClinVar RCV Id: RCV001288973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala385Pro
CA367398729
NM_033507.3:c.1153G>C