Allele Registry

Canonical Allele Identifier: PA098863

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006168

ClinVar Variation:

5812

HGVS (amino-acid)	Matching Registered Transcripts
NP_620594.1:p.Arg268Pro	CA117776 NM_139025.5:c.803G>C