Allele Registry

Canonical Allele Identifier: PA2830271986

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006170

RCV000251648

RCV000767050

ClinVar Variation:

5814

HGVS (amino-acid)	Matching Registered Transcripts
NP_620595.1:p.Pro444Ser	CA117779 NM_139026.6:c.1330C>T