Allele Registry

Canonical Allele Identifier: PA127066

Gene: C3 HGNC NCBI

ClinVar RCV:

RCV000018586

RCV000286026

RCV000321048

RCV000380392

RCV001515572

RCV002293985

RCV002371776

ClinVar Variation:

17057

HGVS (amino-acid)	Matching Registered Transcripts
NP_000055.2:p.Pro314Leu	CA127064 NM_000064.4:c.941C>T