Allele Registry

Canonical Allele Identifier: PA2741813055

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV003480457

ClinVar Variation:

2683637

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Thr1217del	CA1305997 NM_000186.4:c.3649_3651del