Canonical Allele Identifier: PA2825096506
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1968602
ClinVar RCV Id: RCV002711912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Val414Ile
CA35824807
NM_000186.4:c.1240G>A