Allele Registry

Canonical Allele Identifier: PA916071891

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006158

ClinVar Variation:

5802

HGVS (amino-acid)	Matching Registered Transcripts
NP_620596.2:p.Arg398His	CA117751 NM_139027.6:c.1193G>A