Allele Registry

Canonical Allele Identifier: PA2825084069

Gene: CFI HGNC NCBI

ClinVar Allele:

27161

ClinVar RCV:

RCV000012905

ClinVar Variation:

12122

HGVS (amino-acid)	Matching Registered Transcripts
NP_000195.3:p.Asp524Val	CA256214 NM_000204.5:c.1571A>T