Canonical Allele Identifier: PA2499227706
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1050379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Val1252Ile
CA9128645
NM_000064.4:c.3754G>A