Canonical Allele Identifier: PA2499229570
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 988220
ClinVar RCV Id: RCV001328247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Thr1216Lys
CA343988268
NM_000186.4:c.3647C>A