Canonical Allele Identifier: PA2573160481
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484694
ClinVar RCV Id: RCV002038131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Asp1440Asn
CA9128438
NM_000064.4:c.4318G>A