Canonical Allele Identifier: PA2827353087
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1509573
ClinVar RCV Id: RCV002040708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317964.1:p.Ile571Thr
CA3041832
NM_001331035.2:c.1712T>C