Allele Registry

Canonical Allele Identifier: PA3057495839

Gene: CFB HGNC NCBI

ClinVar RCV:

RCV005075817

ClinVar Variation:

3616154

HGVS (amino-acid)	Matching Registered Transcripts
NP_001701.2:p.Gly568Glu	CA363408991 NM_001710.6:c.1703G>A