Canonical Allele Identifier: PA2825096395
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_000177.2:p.Phe176Leu
CA1305084
NM_000186.4:c.526T>C
CA343977182
NM_000186.4:c.528T>A
CA343977183
NM_000186.4:c.528T>G