Canonical Allele Identifier: PA2573060342
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1311296
ClinVar RCV Id: RCV001758805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Ser1401Thr
CA403615466
NM_000064.4:c.4201T>A