Allele Registry

Canonical Allele Identifier: PA098974

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV000059755

ClinVar Variation:

68803

HGVS (amino-acid)	Matching Registered Transcripts
NP_620594.1:p.Cys508Tyr	CA219986 NM_139025.5:c.1523G>A