Canonical Allele Identifier: PA2827937038
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser433_Ile436del
CA2580617739
NM_001354800.1:c.1298_1309del