Canonical Allele Identifier: PA2741810968
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2780822
ClinVar RCV Id: RCV003659636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Gln1226His
CA403620062
NM_000064.4:c.3678G>T
CA403620066
NM_000064.4:c.3678G>C