Canonical Allele Identifier: PA2830122790
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1502971
ClinVar RCV Id: RCV002022599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg62Leu
CA367403268
NM_033508.3:c.185G>T