Canonical Allele Identifier: PA2573160466
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1487278
ClinVar RCV Id: RCV002006340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Asp1216Ala
CA403620316
NM_000064.4:c.3647A>C