Allele Registry

Canonical Allele Identifier: PA095197

Gene: C3 HGNC NCBI

ClinVar RCV:

RCV000018591

RCV002513105

ClinVar Variation:

17062

HGVS (amino-acid)	Matching Registered Transcripts
NP_000055.2:p.Asp1115Asn	CA257695 NM_000064.4:c.3343G>A