Canonical Allele Identifier: PA2828569416
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2822721
ClinVar RCV Id: RCV003714213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362213.1:p.Met329Val
CA357854616
NM_001375284.1:c.985A>G