Canonical Allele Identifier: PA257495
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 16543
ClinVar RCV Id: RCV000018009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Cys536Arg
CA257493
NM_000186.4:c.1606T>C