Canonical Allele Identifier: PA2830124012
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe422Ser
CA367397256
NM_033508.3:c.1265T>C