Canonical Allele Identifier: PA645460257
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg251Cys
CA16609268
NM_033507.3:c.751C>T