Canonical Allele Identifier: PA2830122696
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg42His
CA4239718
NM_033508.3:c.125G>A