Canonical Allele Identifier: PA2741811000
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2809822
ClinVar RCV Id: RCV003680148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Met1400Val
CA403615482
NM_000064.4:c.4198A>G