Canonical Allele Identifier: PA2580103320
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1712462
ClinVar RCV Id: RCV002294717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Phe830del
CA2580613031
NM_000064.4:c.2488_2490del