Canonical Allele Identifier: PA2741885692
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 2955658
ClinVar RCV Id: RCV003810809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Arg605Gln
CA136897928
NM_001710.6:c.1814G>A