Allele Registry

Canonical Allele Identifier: PA916021957

Gene: C5 HGNC NCBI

ClinVar RCV:

RCV000454843

RCV001509919

ClinVar Variation:

402454

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304092.1:p.Val808Ile	CA5217784 NM_001317163.2:c.2422G>A