Canonical Allele Identifier: PA1139685673
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 894696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Leu1318Arg
CA9128591
NM_000064.4:c.3953T>G