Canonical Allele Identifier: PA2828568651
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1718685
ClinVar RCV Id: RCV002301593
ClinVar Variation Id: 2111996
ClinVar RCV Id: RCV003024112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362210.1:p.Asn464Lys
CA3041925
NM_001375281.1:c.1392T>G
CA357856625
NM_001375281.1:c.1392T>A