Allele Registry

Canonical Allele Identifier: PA916071869

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006168

ClinVar Variation:

5812

HGVS (amino-acid)	Matching Registered Transcripts
NP_620596.2:p.Arg268Pro	CA117776 NM_139027.6:c.803G>C