Canonical Allele Identifier: PA2830122812
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36209
ClinVar Variation Id: 976334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly71Arg
CA213771
NM_033508.3:c.211G>A
CA367403112
NM_033508.3:c.211G>C