Canonical Allele Identifier: PA2827936558
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136526
ClinVar RCV Id: RCV003037221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser151Pro
CA367401938
NM_001354800.1:c.451T>C