Canonical Allele Identifier: PA2579974558
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1801853
ClinVar RCV Id: RCV002464672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val33Gly
CA367403603
NM_000162.5:c.98T>G