Canonical Allele Identifier: PA2827937374
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala65Val
CA213727
NM_001354803.2:c.194C>T