Canonical Allele Identifier: PA2829340939
Gene: C5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2083369
ClinVar RCV Id: RCV003002478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001726.2:p.Lys1456Asn
CA5217192
NM_001735.3:c.4368A>C
CA374747451
NM_001735.3:c.4368A>T