Allele Registry

Canonical Allele Identifier: PA2580255982

Gene: CFB HGNC NCBI

ClinVar RCV:

RCV002842924

RCV004064943

ClinVar Variation:

2010098

HGVS (amino-acid)	Matching Registered Transcripts
NP_001701.2:p.Ala567Gly	CA363408978 NM_001710.6:c.1700C>G