Canonical Allele Identifier: PA916028669
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 372807
ClinVar RCV Id: RCV000413659 RCV003144247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317964.1:p.Asn151Ser
CA3042272
NM_001331035.2:c.452A>G