Canonical Allele Identifier: PA257518
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 16555
ClinVar RCV Id: RCV000018022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Lys224del
CA257516
NM_000186.4:c.671_673del
CA343977763
NM_000186.4:c.670A>T