Canonical Allele Identifier: PA658805993
Gene: CFHR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 523008
ClinVar RCV Id: RCV000626208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066303.2:p.Cys268Phe
CA1306293
NM_021023.5:c.803G>T