Canonical Allele Identifier: PA2580103358
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721989
ClinVar RCV Id: RCV002295067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Ala876Thr
CA403633349
NM_000064.4:c.2626G>A