Canonical Allele Identifier: PA2825083933
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2833866
ClinVar RCV Id: RCV003692214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000195.3:p.Pro451Arg
CA103689342
NM_000204.5:c.1352C>G