Allele Registry

Canonical Allele Identifier: PA098913

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006165

RCV002512822

ClinVar Variation:

5809

HGVS (amino-acid)	Matching Registered Transcripts
NP_620594.1:p.Arg692Cys	CA117769 NM_139025.5:c.2074C>T