Canonical Allele Identifier: PA2499227688
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1163120
ClinVar RCV Id: RCV001507920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Gln276Glu
CA9129657
NM_000064.4:c.826C>G