Canonical Allele Identifier: PA915956522
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 16551
ClinVar RCV Id: RCV000018018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014975.1:p.Cys431Ser
CA257506
NM_001014975.3:c.1291T>A
CA343980786
NM_001014975.3:c.1292G>C