Canonical Allele Identifier: PA2825096278
Gene: CFH HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Leu4Pro
CA343988826
NM_000186.4:c.11T>C