Canonical Allele Identifier: PA658802688
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 522442
ClinVar RCV Id: RCV000625583 RCV003669163 RCV003333088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Asp20Asn
CA343989152
NM_000186.4:c.58G>A