Allele Registry

Canonical Allele Identifier: PA2741810776

Gene: C3 HGNC NCBI

ClinVar RCV:

RCV003675054

ClinVar Variation:

2794813

HGVS (amino-acid)	Matching Registered Transcripts
NP_000055.2:p.Lys65Glu	CA403646023 NM_000064.4:c.193A>G