Canonical Allele Identifier: PA2580107596
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 2329373
ClinVar RCV Id: RCV002924630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Gly557Ala
CA343983688
NM_000186.4:c.1670G>C