Canonical Allele Identifier: PA126180
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 16075
ClinVar RCV Id: RCV000017454 RCV000017453 RCV000017458 RCV000259759 RCV000319518 RCV000281261 RCV000455762 RCV001515636 RCV001154197 RCV002504800 RCV002293980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Arg32Gln
CA126178
NM_001710.6:c.95G>A