Canonical Allele Identifier: PA2573175874
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1358876
ClinVar RCV Id: RCV001872113 RCV002489983 RCV003452005 RCV003452006 RCV003452003 RCV003452004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001014975.1:p.Phe176Leu
CA1305084
NM_001014975.3:c.526T>C
CA343977182
NM_001014975.3:c.528T>A
CA343977183
NM_001014975.3:c.528T>G