Canonical Allele Identifier: PA2827937358
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 908615
ClinVar RCV Id: RCV001159192 RCV001159193 RCV001159194 RCV001160541 RCV002483905 RCV003493804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Thr20Pro
CA157913750
NM_001354803.2:c.58A>C