Canonical Allele Identifier: PA2830122656
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664358
ClinVar RCV Id: RCV003445456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met36Val
CA367403551
NM_033508.3:c.106A>G