Canonical Allele Identifier: PA2827937442
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala134Val
CA257433
NM_001354803.2:c.401C>T