Canonical Allele Identifier: PA645425237
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 294513
ClinVar RCV Id: RCV000307054 RCV000341877 RCV000347912 RCV000408202 RCV002294236 RCV001850510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Gly1002Arg
CA1305806
NM_000186.4:c.3004G>C
CA343981428
NM_000186.4:c.3004G>A