Canonical Allele Identifier: PA2741810886
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2880080
ClinVar RCV Id: RCV003713115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.His868Pro
CA9129013
NM_000064.4:c.2603A>C