Canonical Allele Identifier: PA916039374
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ala76Val
CA257433
NM_001354802.1:c.227C>T