Canonical Allele Identifier: PA916039359
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ala7Glu
CA213725
NM_001354802.1:c.20C>A