Canonical Allele Identifier: PA2825084084
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2891695
ClinVar RCV Id: RCV003725072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000195.3:p.Gly542Ser
CA3041853
NM_000204.5:c.1624G>A