Canonical Allele Identifier: PA2573296696
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1365290
ClinVar RCV Id: RCV001942615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ile226Thr
CA367401133
NM_033507.3:c.677T>C