Canonical Allele Identifier: PA2827936928
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 429640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg377_Ala379del
CA645369436
NM_001354800.1:c.1130_1138del