Allele Registry

Canonical Allele Identifier: PA126183

Gene: CFB HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000017455

RCV000293644

RCV000324324

RCV000324934

RCV001154196

RCV001510498

RCV002293981

RCV002496388

RCV004549373

ClinVar Variation:

16076

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001701.2:p.Arg32Trp	CA126181 NM_001710.6:c.94C>T