Canonical Allele Identifier: PA891855359
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585909
ClinVar RCV Id: RCV000711758 RCV002285406 RCV003420270 RCV003318504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg393Cys
CA367398622
NM_033507.3:c.1177C>T