Canonical Allele Identifier: PA220089
Gene: CFHR5 HGNC NCBI

Linked Data

ClinVar Variation Id: 68846
ClinVar RCV Id: RCV000059809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110414.1:p.Tyr277Asn
CA220087
NM_030787.4:c.829T>A