Canonical Allele Identifier: PA2741810891
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3001428
ClinVar RCV Id: RCV003852571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Pro890His
CA9129004
NM_000064.4:c.2669C>A