Canonical Allele Identifier: PA2499235174
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1032243
ClinVar RCV Id: RCV001334297 RCV001507510 RCV002476550 RCV003449950 RCV003449952 RCV003449951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014975.1:p.Arg166Gln
CA1305079
NM_001014975.3:c.497G>A