Canonical Allele Identifier: PA2830123736
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 450453
ClinVar RCV Id: RCV000520175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr331Arg
CA367399765
NM_033508.3:c.992C>G