Allele Registry

Canonical Allele Identifier: PA916071822

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006154

ClinVar Variation:

5798

HGVS (amino-acid)	Matching Registered Transcripts
NP_620596.2:p.His96Asp	CA117739 NM_139027.6:c.286C>G