Canonical Allele Identifier: PA2573160468
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1419844
ClinVar RCV Id: RCV001940752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Pro1223Leu
CA403620131
NM_000064.4:c.3668C>T