Canonical Allele Identifier: PA2827936554
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3068510
ClinVar RCV Id: RCV003993702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Phe150Leu
CA367401941
NM_001354800.1:c.450C>G
CA367401942
NM_001354800.1:c.450C>A
CA367401948
NM_001354800.1:c.448T>C