Canonical Allele Identifier: PA645467895
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 356292
ClinVar RCV Id: RCV000272181 RCV000364523 RCV002294321 RCV001518263 RCV004549808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Lys565Glu
CA3728432
NM_001710.6:c.1693A>G