Allele Registry

Canonical Allele Identifier: PA099166

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006157

RCV001507764

ClinVar Variation:

5801

HGVS (amino-acid)	Matching Registered Transcripts
NP_620594.1:p.Thr196Ile	CA117748 NM_139025.5:c.587C>T