Canonical Allele Identifier: PA1139685648
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 892708
ClinVar RCV Id: RCV001129148 RCV001129147 RCV001129149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Gly1265Ser
CA403619399
NM_000064.4:c.3793G>A