Canonical Allele Identifier: PA1139685465
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 892936
ClinVar RCV Id: RCV001129882 RCV001130593 RCV001129883 RCV001856689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Glu279Lys
CA9129654
NM_000064.4:c.835G>A