Canonical Allele Identifier: PA2580103591
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2414219
ClinVar RCV Id: RCV003106552
ClinVar Variation Id: 2978868
ClinVar RCV Id: RCV003839514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Gly1394Arg
CA9128477
NM_000064.4:c.4180G>C
CA9128478
NM_000064.4:c.4180G>A