Allele Registry

Canonical Allele Identifier: PA2830272070

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000244738

RCV000345892

RCV001651270

ClinVar Variation:

262430

HGVS (amino-acid)	Matching Registered Transcripts
NP_620595.1:p.Pro587Ala	CA10587034 NM_139026.6:c.1759C>G