Allele Registry

Canonical Allele Identifier: PA2828569410

Gene: CFI HGNC NCBI

ClinVar Allele:

3395098

ClinVar RCV:

RCV004555240

ClinVar Variation:

3235979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362213.1:p.Asp321Gly	CA357854665 NM_001375284.1:c.962A>G