Canonical Allele Identifier: PA2580103180
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2029044
ClinVar RCV Id: RCV002876445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Pro238Ala
CA304798523
NM_000064.4:c.712C>G