Allele Registry

Canonical Allele Identifier: PA916071929

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000244738

RCV000345892

RCV001651270

ClinVar Variation:

262430

HGVS (amino-acid)	Matching Registered Transcripts
NP_620596.2:p.Pro618Ala	CA10587034 NM_139027.6:c.1852C>G