Canonical Allele Identifier: PA2580131827
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 2181560
ClinVar RCV Id: RCV002606210
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014975.1:p.Ile184Thr
CA1305088
NM_001014975.3:c.551T>C