Canonical Allele Identifier: PA645425154
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 294495
ClinVar RCV Id: RCV000282381 RCV000317574 RCV000336971 RCV000372197 RCV001850509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Val579Ala
CA1305475
NM_000186.4:c.1736T>C