Canonical Allele Identifier: PA2827936384
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2504386
ClinVar RCV Id: RCV003231847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu20Pro
CA367403809
NM_001354800.1:c.59T>C