Canonical Allele Identifier: PA2573198611
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1431614
ClinVar RCV Id: RCV001967578
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304986.2:p.Gly524Val
CA3041862
NM_001318057.2:c.1571G>T