ClinGen Allele Registry
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Canonical Allele Identifier:
PA128565
Gene: CFH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000018025
RCV000018026
RCV000022540
RCV001099303
RCV001099304
RCV001328126
RCV001508947
RCV001536004
RCV002293983
ClinVar Variation:
16558
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000177.2:p.Arg1210Cys
CA128563
NM_000186.4:c.3628C>T