Canonical Allele Identifier: PA2827353017
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 1718685
ClinVar RCV Id: RCV002301593
ClinVar Variation Id: 2111996
ClinVar RCV Id: RCV003024112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317964.1:p.Asn457Lys
CA3041925
NM_001331035.2:c.1371T>G
CA357856625
NM_001331035.2:c.1371T>A