Canonical Allele Identifier: PA645425211
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 294510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Gln950His
CA1305760
NM_000186.4:c.2850G>T
CA343981075
NM_000186.4:c.2850G>C