Canonical Allele Identifier: PA2580103361
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087385
ClinVar RCV Id: RCV003017837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Gln883Glu
CA403633191
NM_000064.4:c.2647C>G