Canonical Allele Identifier: PA2580107594
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1693689
ClinVar RCV Id: RCV002261558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Tyr540Cys
CA343983360
NM_000186.4:c.1619A>G