Canonical Allele Identifier: PA658669098
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447424
ClinVar RCV Id: RCV000517815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg304Leu
CA367400050
NM_033507.3:c.911G>T