Allele Registry

Canonical Allele Identifier: PA645466288

Gene: FBXW7 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419727

RCV000421731

RCV000422964

RCV000423635

RCV000425901

RCV000430408

RCV000431029

RCV000431539

RCV000434382

RCV000436100

RCV000440224

RCV000441781

RCV000443518

RCV000443662

ClinVar Variation:

376417

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_361014.1:p.Arg465Leu	CA16602854 NM_033632.3:c.1394G>T