Canonical Allele Identifier: PA915956511
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 625915
ClinVar RCV Id: RCV000767926 RCV000788892 RCV001098523 RCV001098524 RCV001096771 RCV001096772 RCV003453584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014975.1:p.Ala161Ser
CA1305074
NM_001014975.3:c.481G>T