Canonical Allele Identifier: PA2580490839
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136513
ClinVar RCV Id: RCV003037215
ClinVar Variation Id: 2735003
ClinVar RCV Id: RCV003555334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp279Glu
CA367400460
NM_033507.3:c.837C>G
CA367400461
NM_033507.3:c.837C>A