Canonical Allele Identifier: PA2830121334
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3234001
ClinVar RCV Id: RCV004527577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.His157Asp
CA367401894
NM_033507.3:c.469C>G