Canonical Allele Identifier: PA2579976570
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136526
ClinVar RCV Id: RCV003037221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser151Pro
CA367401938
NM_000162.5:c.451T>C