Canonical Allele Identifier: PA645459510
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36209
ClinVar Variation Id: 976334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly73Arg
CA213771
NM_033507.3:c.217G>A
CA367403112
NM_033507.3:c.217G>C