Allele Registry

Canonical Allele Identifier: PA095137

Gene: C3 HGNC NCBI

ClinVar RCV:

RCV000018590

ClinVar Variation:

17061

HGVS (amino-acid)	Matching Registered Transcripts
NP_000055.2:p.Ala1094Val	CA257693 NM_000064.4:c.3281C>T