Canonical Allele Identifier: PA2825096497
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1006921
ClinVar RCV Id: RCV001304040 RCV001332256 RCV002499567 RCV003449864 RCV003449865 RCV003449866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Gln400Lys
CA1305282
NM_000186.4:c.1198C>A