Allele Registry

Canonical Allele Identifier: PA098907

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000006160

RCV003480021

ClinVar Variation:

5804

HGVS (amino-acid)	Matching Registered Transcripts
NP_620594.1:p.Arg528Gly	CA117757 NM_139025.5:c.1582A>G