Canonical Allele Identifier: PA916039386
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 429640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg55_Ala57del
CA645369436
NM_001354803.2:c.164_172del