Canonical Allele Identifier: PA2741810835
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2535518
ClinVar RCV Id: RCV003261050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Ser567Thr
CA403639614
NM_000064.4:c.1700G>C