Canonical Allele Identifier: PA2499229562
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 988144
ClinVar RCV Id: RCV001328127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Asn1178Tyr
CA343987268
NM_000186.4:c.3532A>T