Canonical Allele Identifier: PA2580103262
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1926422
ClinVar RCV Id: RCV002605180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Val565Leu
CA9129353
NM_000064.4:c.1693G>C
CA403639638
NM_000064.4:c.1693G>T
CA2580097030
NM_000064.4:c.1692_1693delinsAC