Allele Registry

Canonical Allele Identifier: PA2826958097

Gene: C5 HGNC NCBI

ClinVar RCV:

RCV000018581

ClinVar Variation:

17053

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304093.1:p.Lys372Arg	CA127058 NM_001317164.2:c.1115A>G