Allele Registry

Canonical Allele Identifier: PA151358

Gene: C5 HGNC NCBI

ClinVar RCV:

RCV000114935

RCV001854541

RCV002483183

ClinVar Variation:

127072

HGVS (amino-acid)	Matching Registered Transcripts
NP_001726.2:p.Arg885Cys	CA151356 NM_001735.3:c.2653C>T