Canonical Allele Identifier: PA2573160475
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1388745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Arg1393Trp
CA9128481
NM_000064.4:c.4177C>T