Allele Registry

Canonical Allele Identifier: PA098944

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006164

ClinVar Variation:

5808

HGVS (amino-acid)	Matching Registered Transcripts
NP_620594.1:p.Cys1213Tyr	CA117766 NM_139025.5:c.3638G>A