Canonical Allele Identifier: PA2580103506
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1910079
ClinVar RCV Id: RCV002592996 RCV002592997
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Pro1223Ser
CA9128663
NM_000064.4:c.3667C>T