Canonical Allele Identifier: PA2580490780
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1743101
ClinVar RCV Id: RCV002330710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp161His
CA367401848
NM_033507.3:c.481G>C