Canonical Allele Identifier: PA645425200
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 294509
ClinVar RCV Id: RCV000272281 RCV000307823 RCV000362551 RCV000406400 RCV001513114 RCV001579061 RCV001701991 RCV002294233 RCV002494911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Glu936Asp
CA1305755
NM_000186.4:c.2808G>T
CA343980982
NM_000186.4:c.2808G>C