Canonical Allele Identifier: PA658668991
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447409
ClinVar RCV Id: RCV000518379 RCV002463702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met198Thr
CA367401431
NM_033507.3:c.593T>C