Allele Registry

Canonical Allele Identifier: PA2825083603

Gene: CFI HGNC NCBI

ClinVar RCV:

RCV000413659

RCV003144247

ClinVar Variation:

372807

HGVS (amino-acid)	Matching Registered Transcripts
NP_000195.3:p.Asn151Ser	CA3042272 NM_000204.5:c.452A>G