Allele Registry

Canonical Allele Identifier: PA658655397

Gene: FBXW7 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417428

RCV000418970

RCV000422698

RCV000424610

RCV000424801

RCV000427741

RCV000428799

RCV000433446

RCV000434066

RCV000435527

RCV000436201

RCV000440831

RCV000442912

RCV000443932

ClinVar Variation:

376416

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_060785.2:p.Arg385Pro	CA16602853 NM_018315.5:c.1154G>C