Allele Registry

Canonical Allele Identifier: PA891866339

Gene: FBXW7 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417744

RCV000417975

RCV000420844

RCV000422069

RCV000426392

RCV000427168

RCV000428675

RCV000429314

RCV000433642

RCV000437827

RCV000437932

RCV000438452

RCV000439989

RCV000443195

ClinVar Variation:

376415

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336727.1:p.Arg465His	CA16602852 NM_001349798.2:c.1394G>A