Canonical Allele Identifier: PA2573061759
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1342904
ClinVar RCV Id: RCV001842261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Arg1206Cys
CA343988072
NM_000186.4:c.3616C>T