Canonical Allele Identifier: PA257508
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_000177.2:p.Cys431Ser
CA257506
NM_000186.4:c.1291T>A
CA343980786
NM_000186.4:c.1292G>C