Allele Registry

Canonical Allele Identifier: PA275484

Gene: C3 HGNC NCBI

ClinVar RCV:

RCV000184049

RCV003727628

ClinVar Variation:

202203

HGVS (amino-acid)	Matching Registered Transcripts
NP_000055.2:p.Pro214Ser	CA275482 NM_000064.4:c.640C>T