Allele Registry

Canonical Allele Identifier: PA916071988

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000059767

RCV000779576

RCV002469002

RCV003952487

ClinVar Variation:

68815

HGVS (amino-acid)	Matching Registered Transcripts
NP_620596.2:p.Arg1060Trp	CA220022 NM_139027.6:c.3178C>T