Canonical Allele Identifier: PA2825096494
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1723621
ClinVar RCV Id: RCV002308895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Lys388Asn
CA343980504
NM_000186.4:c.1164A>C
CA343980505
NM_000186.4:c.1164A>T