Allele Registry

Canonical Allele Identifier: PA916071838

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000778929

RCV001507763

RCV003994114

ClinVar Variation:

632074

HGVS (amino-acid)	Matching Registered Transcripts
NP_620596.2:p.Asp187His	CA200922204 NM_139027.6:c.559G>C