Canonical Allele Identifier: PA2741868034
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2628365
ClinVar RCV Id: RCV003397220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala56Pro
CA367398808
NM_001354803.2:c.166G>C