Canonical Allele Identifier: PA2827936722
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 381599
ClinVar RCV Id: RCV000419860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met235Val
CA16605219
NM_001354800.1:c.703A>G