Canonical Allele Identifier: PA2828569223
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2119609
ClinVar RCV Id: RCV003033178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362212.1:p.Ala515Val
CA357854595
NM_001375283.1:c.1544C>T