Canonical Allele Identifier: PA2830123919
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1522625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg393Leu
CA367398578
NM_033508.3:c.1178G>T