Canonical Allele Identifier: PA915956520
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 294490
ClinVar RCV Id: RCV000296616 RCV000327040 RCV000349294 RCV000388493 RCV001579193 RCV001521610 RCV002294225
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Amino-acid Alleles

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