Canonical Allele Identifier: PA645406570
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 330292
ClinVar RCV Id: RCV000279638 RCV000338521 RCV000396966 RCV000788906 RCV001727686 RCV003910272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Gly1224Asp
CA9128662
NM_000064.4:c.3671G>A