Canonical Allele Identifier: PA2827936934
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala379Gly
CA367398793
NM_001354800.1:c.1136C>G