Canonical Allele Identifier: PA2573220201
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 1422280
ClinVar RCV Id: RCV001919454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Arg50Gln
CA3727959
NM_001710.6:c.149G>A