Canonical Allele Identifier: PA2573164294
Gene: CFH HGNC NCBI

Linked Data

ClinVar Variation Id: 1361265
ClinVar RCV Id: RCV001907438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000177.2:p.Ile563Thr
CA1305454
NM_000186.4:c.1688T>C