Canonical Allele Identifier: PA2580107638
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1693711
ClinVar RCV Id: RCV002261580 RCV002505902 RCV003454053 RCV003454054 RCV003454055 RCV003454056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Val1054Ile
CA1305863
NM_000186.4:c.3160G>A