Canonical Allele Identifier: PA2827937272
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ala4Glu
CA367398725
NM_001354802.1:c.11C>A