Canonical Allele Identifier: PA2828569220
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2819958
ClinVar RCV Id: RCV003706536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362212.1:p.Gly508Val
CA357854644
NM_001375283.1:c.1523G>T