Allele Registry

Canonical Allele Identifier: PA916021958

Gene: C5 HGNC NCBI

ClinVar RCV:

RCV000114935

RCV001854541

RCV002483183

ClinVar Variation:

127072

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304092.1:p.Arg891Cys	CA151356 NM_001317163.2:c.2671C>T