Canonical Allele Identifier: PA2573160467
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1348619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Arg1219Cys
CA9128666
NM_000064.4:c.3655C>T