Canonical Allele Identifier: PA658668951
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 451640
ClinVar Variation Id: 2921032
ClinVar RCV Id: RCV003740508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu145Pro
CA367401995
NM_033507.3:c.434T>C
CA2695202965
NM_033507.3:c.434_435delinsCT