Canonical Allele Identifier: PA2830123778
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 381598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val366Met
CA16605802
NM_033508.3:c.1096G>A