Canonical Allele Identifier: PA2827937378
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3061155
ClinVar RCV Id: RCV003982667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Glu73_Arg81del
CA574226172
NM_001354803.2:c.217_243del