Allele Registry

Canonical Allele Identifier: PA3057450393

Gene: CFH HGNC NCBI

ClinVar RCV:

RCV005013351

ClinVar Variation:

3575710

HGVS (amino-acid)	Matching Registered Transcripts
NP_000177.2:p.Thr1184Ile	CA343987465 NM_000186.4:c.3551C>T