Canonical Allele Identifier: PA2580490767
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136526
ClinVar RCV Id: RCV003037221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ser152Pro
CA367401938
NM_033507.3:c.454T>C