Canonical Allele Identifier: PA2827937001
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233996
ClinVar RCV Id: RCV004527572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly410Cys
CA367398311
NM_001354800.1:c.1228G>T