Canonical Allele Identifier: PA2573160438
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1381503
ClinVar RCV Id: RCV001895394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Arg855Gln
CA9129038
NM_000064.4:c.2564G>A