Allele Registry

Canonical Allele Identifier: PA2830271830

Gene: ADAMTS13 HGNC NCBI

ClinVar Allele:

20840

ClinVar RCV:

RCV000006157

RCV001507764

ClinVar Variation:

5801

HGVS (amino-acid)	Matching Registered Transcripts
NP_620595.1:p.Thr196Ile	CA117748 NM_139026.6:c.587C>T