Canonical Allele Identifier: PA2573160413
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1378200
ClinVar RCV Id: RCV001881022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Arg573Trp
CA304794584
NM_000064.4:c.1717C>T