Canonical Allele Identifier: PA2579977057
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 381599
ClinVar RCV Id: RCV000419860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met235Val
CA16605219
NM_000162.5:c.703A>G