Canonical Allele Identifier: PA2827937339
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Phe43Ser
CA367397256
NM_001354802.1:c.128T>C