Canonical Allele Identifier: PA2580103502
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2152301
ClinVar RCV Id: RCV003079225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Arg1219His
CA9128664
NM_000064.4:c.3656G>A