Canonical Allele Identifier: PA645425234
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 265982
ClinVar RCV Id: RCV000256395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Cys984Arg
CA10588915
NM_000186.4:c.2950T>C