Canonical Allele Identifier: PA2830121304
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3068510
ClinVar RCV Id: RCV003993702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe151Leu
CA367401941
NM_033507.3:c.453C>G
CA367401942
NM_033507.3:c.453C>A
CA367401948
NM_033507.3:c.451T>C