Canonical Allele Identifier: PA2830123940
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1303093
ClinVar RCV Id: RCV001756592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val405Met
CA367398367
NM_033508.3:c.1213G>A