Canonical Allele Identifier: PA2825096509
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 2983085
ClinVar RCV Id: RCV003847700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Tyr420His
CA1305291
NM_000186.4:c.1258T>C