Canonical Allele Identifier: PA2830123886
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala386Val
CA213727
NM_033508.3:c.1157C>T