Canonical Allele Identifier: PA2580103179
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1968266
ClinVar RCV Id: RCV002755142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Val228Met
CA403643093
NM_000064.4:c.682G>A