Canonical Allele Identifier: PA2580107593
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1927291
ClinVar RCV Id: RCV002631096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Thr504Arg
CA1305405
NM_000186.4:c.1511C>G