Canonical Allele Identifier: PA2741810805
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2881190
ClinVar RCV Id: RCV003715806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Ala316Val
CA403642160
NM_000064.4:c.947C>T