Canonical Allele Identifier: PA2826033810
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_001160096.1:p.Cys207Phe
CA1306293
NM_001166624.2:c.620G>T