Canonical Allele Identifier: PA2741812962
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 2961744
ClinVar RCV Id: RCV003822390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Ala484Glu
CA343982106
NM_000186.4:c.1451C>A