Canonical Allele Identifier: PA2579983158
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala384Glu
CA367398725
NM_000162.5:c.1151C>A