Canonical Allele Identifier: PA2580103607
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2160017
ClinVar RCV Id: RCV003087522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Arg1491Gln
CA9128376
NM_000064.4:c.4472G>A