Canonical Allele Identifier: PA2573160434
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1405086
ClinVar RCV Id: RCV001927904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Arg841Gln
CA9129049
NM_000064.4:c.2522G>A