Canonical Allele Identifier: PA2741868035
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala56Asp
CA367398804
NM_001354803.2:c.167C>A