Canonical Allele Identifier: PA2830122699
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585913
ClinVar RCV Id: RCV000711764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg42Pro
CA367403448
NM_033508.3:c.125G>C