Allele Registry

Canonical Allele Identifier: PA916071956

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000220213

RCV002054940

RCV002485379

ClinVar Variation:

227176

HGVS (amino-acid)	Matching Registered Transcripts
NP_620596.2:p.Ala732Val	CA10576747 NM_139027.6:c.2195C>T