Canonical Allele Identifier: PA916039373
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Val75Met
CA257432
NM_001354802.1:c.223G>A