Canonical Allele Identifier: PA2830123717
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447426
ClinVar Variation Id: 2861776
ClinVar RCV Id: RCV003704517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.His316Gln
CA367399915
NM_033508.3:c.948C>G
CA367399916
NM_033508.3:c.948C>A