Canonical Allele Identifier: PA2579981941
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 450262
ClinVar Variation Id: 1045215
ClinVar RCV Id: RCV001349584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asn254Lys
CA367400610
NM_000162.5:c.762T>G
CA367400611
NM_000162.5:c.762T>A