Allele Registry

Canonical Allele Identifier: PA658655398

Gene: FBXW7 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000420440

RCV000420611

RCV000421110

RCV000422617

RCV000426601

RCV000428525

RCV000431273

RCV000431798

RCV000432242

RCV000433796

RCV000439190

RCV000439851

RCV000441161

RCV000443314

RCV002512102

ClinVar Variation:

376414

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_060785.2:p.Arg385Cys	CA16602851 NM_018315.5:c.1153C>T