Canonical Allele Identifier: PA2827936635
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 283358
ClinVar RCV Id: RCV000711776 RCV002285302 RCV002222471 RCV002347992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg191Gln
CA10604473
NM_001354800.1:c.572G>A