Canonical Allele Identifier: PA2573160476
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1345571
ClinVar RCV Id: RCV002049882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Ala1398Gly
CA403615502
NM_000064.4:c.4193C>G