Canonical Allele Identifier: PA2741810902
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2867816
ClinVar RCV Id: RCV003702967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Val925Ile
CA403632594
NM_000064.4:c.2773G>A