Canonical Allele Identifier: PA341618
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 21090
ClinVar RCV Id: RCV000020180 RCV001843943 RCV002490396 RCV003450649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Val1197Ala
CA341616
NM_000186.4:c.3590T>C