Canonical Allele Identifier: PA2580255985
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 2478231
ClinVar RCV Id: RCV003209247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Val577Ala
CA363409133
NM_001710.6:c.1730T>C