Canonical Allele Identifier: PA645466295
Gene: FBXW7 HGNC NCBI

Linked Data

ClinVar Variation Id: 376423
ClinVar RCV Id: RCV000420774 RCV000419644 RCV000420999 RCV000425337 RCV000426495 RCV000430756 RCV000431005 RCV000436496 RCV000437332 RCV000438652 RCV000437528 RCV000443509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_361014.1:p.Arg505Gly
CA16602859
NM_033632.3:c.1513C>G