Allele Registry

Canonical Allele Identifier: PA2830271773

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006154

ClinVar Variation:

5798

HGVS (amino-acid)	Matching Registered Transcripts
NP_620595.1:p.His96Asp	CA117739 NM_139026.6:c.286C>G