Canonical Allele Identifier: PA2573160391
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1433256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Val300Ala
CA9129624
NM_000064.4:c.899T>C