Allele Registry

Canonical Allele Identifier: PA2825317254

Gene: FBXW7 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419147

RCV000420198

RCV000421262

RCV000421492

RCV000426581

RCV000428024

RCV000429882

RCV000431326

RCV000436581

RCV000437252

RCV000437918

RCV000439102

RCV000441574

RCV000443495

ClinVar Variation:

376418

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001013433.1:p.Arg347Gly	CA16602855 NM_001013415.2:c.1039C>G