Allele Registry

Canonical Allele Identifier: PA2573220277

Gene: CFB HGNC NCBI

ClinVar RCV:

RCV001988922

ClinVar Variation:

1491824

HGVS (amino-acid)	Matching Registered Transcripts
NP_001701.2:p.Glu566Lys	CA363408952 NM_001710.6:c.1696G>A