Canonical Allele Identifier: PA353565
Gene: CD55 HGNC NCBI

Linked Data

ClinVar Variation Id: 224614
ClinVar RCV Id: RCV000210242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000565.1:p.Ser68Asn
CA353563
NM_000574.5:c.203G>A