Canonical Allele Identifier: PA2826977689
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 420176
ClinVar RCV Id: RCV000479573 RCV001150340 RCV002489157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304986.2:p.Val152Met
CA3042270
NM_001318057.2:c.454G>A