Canonical Allele Identifier: PA645460718
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 381598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val368Met
CA16605802
NM_033507.3:c.1102G>A