Canonical Allele Identifier: PA2741859595
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2891695
ClinVar RCV Id: RCV003725072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304986.2:p.Gly550Ser
CA3041853
NM_001318057.2:c.1648G>A