Canonical Allele Identifier: PA915961015
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 830025
ClinVar RCV Id: RCV001029995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Gln844Arg
CA403633927
NM_000064.4:c.2531A>G