Canonical Allele Identifier: PA2741812961
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 2805595
ClinVar RCV Id: RCV003676842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Val482Leu
CA343982076
NM_000186.4:c.1444G>C
CA343982077
NM_000186.4:c.1444G>T