Canonical Allele Identifier: PA2573060341
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310853
ClinVar RCV Id: RCV001761023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Trp1255Cys
CA9128641
NM_000064.4:c.3765G>C
CA403619538
NM_000064.4:c.3765G>T