Allele Registry

Canonical Allele Identifier: PA151355

Gene: C5 HGNC NCBI

ClinVar RCV:

RCV000114934

RCV001854540

ClinVar Variation:

127071

HGVS (amino-acid)	Matching Registered Transcripts
NP_001726.2:p.Arg885His	CA151353 NM_001735.3:c.2654G>A