Canonical Allele Identifier: PA2825008322
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3065051
ClinVar RCV Id: RCV003990128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Ala914Thr
CA403632761
NM_000064.4:c.2740G>A