Canonical Allele Identifier: PA658669111
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 450453
ClinVar RCV Id: RCV000520175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr333Arg
CA367399765
NM_033507.3:c.998C>G