Canonical Allele Identifier: PA2579979304
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3234001
ClinVar RCV Id: RCV004527577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.His156Asp
CA367401894
NM_000162.5:c.466C>G