Canonical Allele Identifier: PA2828567645
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 372807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362207.1:p.Asn151Ser
CA3042272
NM_001375278.1:c.452A>G