Canonical Allele Identifier: PA2827937138
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995100
ClinVar RCV Id: RCV001288973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ala47Pro
CA367398729
NM_001354801.1:c.139G>C