Canonical Allele Identifier: PA916022203
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_001304986.2:p.Asp527Asn
CA256223
NM_001318057.2:c.1579G>A