Canonical Allele Identifier: PA645425121
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 294487
ClinVar RCV Id: RCV000297641 RCV000312490 RCV000336891 RCV000406363 RCV001859772 RCV002294223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Arg257His
CA1305141
NM_000186.4:c.770G>A