Canonical Allele Identifier: PA2580103198
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2192447
ClinVar RCV Id: RCV002607479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Glu279Ala
CA9129653
NM_000064.4:c.836A>C