Allele Registry

Canonical Allele Identifier: PA2830272827

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006164

ClinVar Variation:

5808

HGVS (amino-acid)	Matching Registered Transcripts
NP_620596.2:p.Cys1157Tyr	CA117766 NM_139027.6:c.3470G>A