Canonical Allele Identifier: PA2580131847
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_001014975.1:p.Val414Ile
CA35824807
NM_001014975.3:c.1240G>A