Canonical Allele Identifier: PA2827936581
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1743101
ClinVar RCV Id: RCV002330710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp160His
CA367401848
NM_001354800.1:c.478G>C