Canonical Allele Identifier: PA2580103590
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2397653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Arg1393Gln
CA9128480
NM_000064.4:c.4178G>A