Canonical Allele Identifier: PA2573220280
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 1462667
ClinVar RCV Id: RCV001985742 RCV002569183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Val577Ile
CA3728436
NM_001710.6:c.1729G>A