Allele Registry

Canonical Allele Identifier: PA117782

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006170

RCV000251648

RCV000767050

ClinVar Variation:

5814

HGVS (amino-acid)	Matching Registered Transcripts
NP_620594.1:p.Pro475Ser	CA117779 NM_139025.5:c.1423C>T