Canonical Allele Identifier: PA2825084106
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1624901
ClinVar RCV Id: RCV002130187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000195.3:p.Pro576Ser
CA3041833
NM_000204.5:c.1726C>T