Canonical Allele Identifier: PA2825084065
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 12126
ClinVar RCV Id: RCV000012909 RCV002512998
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000195.3:p.Asp519Asn
CA256223
NM_000204.5:c.1555G>A