Canonical Allele Identifier: PA2829340937
Gene: C5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2598804
ClinVar RCV Id: RCV004343204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001726.2:p.Thr1451Pro
CA5217193
NM_001735.3:c.4351A>C