Canonical Allele Identifier: PA645406016
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 381739
ClinVar RCV Id: RCV000427027 RCV001328274 RCV003147456 RCV003147457 RCV003320186 RCV003138002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Lys65Gln
CA9129883
NM_000064.4:c.193A>C