Canonical Allele Identifier: PA2830122636
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801853
ClinVar RCV Id: RCV002464672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val32Gly
CA367403603
NM_033508.3:c.95T>G