Canonical Allele Identifier: PA2827936971
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_001341729.1:p.Arg392Cys
CA367398622
NM_001354800.1:c.1174C>T