Allele Registry

Canonical Allele Identifier: PA916071828

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006156

ClinVar Variation:

5800

HGVS (amino-acid)	Matching Registered Transcripts
NP_620596.2:p.Arg102Cys	CA117745 NM_139027.6:c.304C>T