Canonical Allele Identifier: PA645425245
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 294520
ClinVar RCV Id: RCV000298640 RCV000302390 RCV000355977 RCV000403627 RCV001849180 RCV002294240 RCV003454853 RCV001701992 RCV001723878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Asn1050Tyr
CA1305856
NM_000186.4:c.3148A>T