Canonical Allele Identifier: PA916039401
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Asn69Lys
CA367398630
NM_001354803.2:c.207C>G
CA367398633
NM_001354803.2:c.207C>A