Canonical Allele Identifier: PA2830122635
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val32Glu
CA367403606
NM_033508.3:c.95T>A