Canonical Allele Identifier: PA2499229566
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1163685
ClinVar RCV Id: RCV001508944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Glu1198Gly
CA343987919
NM_000186.4:c.3593A>G