Canonical Allele Identifier: PA2573198613
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1509573
ClinVar RCV Id: RCV002040708
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304986.2:p.Ile586Thr
CA3041832
NM_001318057.2:c.1757T>C