Canonical Allele Identifier: PA2580103355
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2086565
ClinVar RCV Id: RCV003015518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Leu867del
CA2580097043
NM_000064.4:c.2600_2602del