Canonical Allele Identifier: PA645425156
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 294497
ClinVar RCV Id: RCV000289073 RCV000309119 RCV000344087 RCV000403698 RCV001317993 RCV002294228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Gly650Val
CA1305536
NM_000186.4:c.1949G>T