Canonical Allele Identifier: PA2827937141
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ala47Glu
CA367398725
NM_001354801.1:c.140C>A