Canonical Allele Identifier: PA2825096392
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1032244
ClinVar RCV Id: RCV001334298 RCV001871860 RCV003449954 RCV003449955 RCV003399118 RCV003449953
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.His169Arg
CA1305082
NM_000186.4:c.506A>G