Canonical Allele Identifier: PA2741859594
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2822721
ClinVar RCV Id: RCV003714213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304986.2:p.Met540Val
CA357854616
NM_001318057.2:c.1618A>G