Canonical Allele Identifier: PA1139685213
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 16555
ClinVar RCV Id: RCV000018022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014975.1:p.Lys224del
CA257516
NM_001014975.3:c.671_673del