Canonical Allele Identifier: PA2827936572
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3234001
ClinVar RCV Id: RCV004527577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.His156Asp
CA367401894
NM_001354800.1:c.466C>G