Canonical Allele Identifier: PA2827936877
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Phe334_Val335delinsLeuMet
CA213696
NM_001354800.1:c.1002_1003delinsAA