Canonical Allele Identifier: PA2827936458
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36209
ClinVar Variation Id: 976334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly72Arg
CA213771
NM_001354800.1:c.214G>A
CA367403112
NM_001354800.1:c.214G>C