Canonical Allele Identifier: PA2580490763
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2428681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu147Pro
CA367401978
NM_033507.3:c.440T>C