Canonical Allele Identifier: PA2827937349
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ser53_Ile56del
CA2580617739
NM_001354802.1:c.158_169del