Canonical Allele Identifier: PA2827937289
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2169517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Arg14Pro
CA367398581
NM_001354802.1:c.41G>C
CA2695203000
NM_001354802.1:c.41_42delinsCG