Canonical Allele Identifier: PA891866341
Gene: FBXW7 HGNC NCBI

Linked Data

ClinVar Variation Id: 376416
ClinVar RCV Id: RCV000417428 RCV000422698 RCV000424610 RCV000424801 RCV000428799 RCV000427741 RCV000435527 RCV000418970 RCV000433446 RCV000436201 RCV000434066 RCV000440831 RCV000442912 RCV000443932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336727.1:p.Arg465Pro
CA16602853
NM_001349798.2:c.1394G>C