Canonical Allele Identifier: PA2579976723
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3068510
ClinVar RCV Id: RCV003993702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe150Leu
CA367401941
NM_000162.5:c.450C>G
CA367401942
NM_000162.5:c.450C>A
CA367401948
NM_000162.5:c.448T>C