Canonical Allele Identifier: PA645467897
Gene: CFB HGNC NCBI

Linked Data

ClinVar Variation Id: 225314
ClinVar RCV Id: RCV000301571 RCV000358897 RCV002294082 RCV004547507 RCV000490470 RCV000987667 RCV001512630
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001701.2:p.Glu566Ala
CA3728434
NM_001710.6:c.1697A>C