Canonical Allele Identifier: PA2827936932
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2628365
ClinVar RCV Id: RCV003397220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala378Pro
CA367398808
NM_001354800.1:c.1132G>C