Canonical Allele Identifier: PA2827936758
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_001341729.1:p.Asn254Lys
CA367400610
NM_001354800.1:c.762T>G
CA367400611
NM_001354800.1:c.762T>A