Canonical Allele Identifier: PA2741825233
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 2983085
ClinVar RCV Id: RCV003847700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014975.1:p.Tyr420His
CA1305291
NM_001014975.3:c.1258T>C