Canonical Allele Identifier: PA2580103516
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2397781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Arg1254His
CA9128642
NM_000064.4:c.3761G>A