Allele Registry

Canonical Allele Identifier: PA915956520

Gene: CFH HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

278205

ClinVar RCV:

RCV000296616

RCV000327040

RCV000349294

RCV000388493

RCV001521610

RCV001579193

RCV002294225

ClinVar Variation:

294490

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001014975.1:p.His402Tyr	CA1305284 NM_001014975.3:c.1204C>T