Allele Registry

Canonical Allele Identifier: PA916021959

Gene: C5 HGNC NCBI

ClinVar RCV:

RCV000114934

RCV001854540

ClinVar Variation:

127071

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304092.1:p.Arg891His	CA151353 NM_001317163.2:c.2672G>A