Canonical Allele Identifier: PA2825084080
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2119609
ClinVar RCV Id: RCV003033178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000195.3:p.Ala534Val
CA357854595
NM_000204.5:c.1601C>T