Canonical Allele Identifier: PA916022197
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 347156
ClinVar RCV Id: RCV000325590 RCV002294306 RCV001512909 RCV001528675 RCV002520195 RCV001849181 RCV003224266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304986.2:p.Lys449Arg
CA3041942
NM_001318057.2:c.1346A>G