Canonical Allele Identifier: PA2829340953
Gene: C5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444152
ClinVar RCV Id: RCV001981684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001726.2:p.Asn1513Ser
CA5217146
NM_001735.3:c.4538A>G