Canonical Allele Identifier: PA2573160444
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1447116
ClinVar RCV Id: RCV001988108 RCV002484761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Pro890Ser
CA9129007
NM_000064.4:c.2668C>T