Allele Registry

Canonical Allele Identifier: PA2830271926

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006158

ClinVar Variation:

5802

HGVS (amino-acid)	Matching Registered Transcripts
NP_620595.1:p.Arg367His	CA117751 NM_139026.6:c.1100G>A