Canonical Allele Identifier: PA2573175901
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1510986
ClinVar RCV Id: RCV002043210
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014975.1:p.Gly435Asp
CA343980815
NM_001014975.3:c.1304G>A