Canonical Allele Identifier: PA2828569407
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_001362213.1:p.Asp316Asn
CA256223
NM_001375284.1:c.946G>A