Canonical Allele Identifier: PA2825096596
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 3236130
ClinVar RCV Id: RCV004555391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Cys564Arg
CA343983771
NM_000186.4:c.1690T>C