Allele Registry

Canonical Allele Identifier: PA916021954

Gene: C5 HGNC NCBI

ClinVar RCV:

RCV000018581

ClinVar Variation:

17053

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304092.1:p.Lys378Arg	CA127058 NM_001317163.2:c.1133A>G