Canonical Allele Identifier: PA2825096511
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 2107927
ClinVar RCV Id: RCV003033892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Ala421Thr
CA1305293
NM_000186.4:c.1261G>A