Canonical Allele Identifier: PA2827936380
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1676825
ClinVar RCV Id: RCV002222321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gln18His
CA367403838
NM_001354800.1:c.54G>T
CA367403840
NM_001354800.1:c.54G>C