Canonical Allele Identifier: PA2580107592
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1994112
ClinVar RCV Id: RCV002806617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Ala501Pro
CA343982425
NM_000186.4:c.1501G>C