Canonical Allele Identifier: PA2827936981
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2169517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg394Pro
CA367398581
NM_001354800.1:c.1181G>C
CA2695203000
NM_001354800.1:c.1181_1182delinsCG