Canonical Allele Identifier: PA2579976367
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe423Ser
CA367397256
NM_000162.5:c.1268T>C