Allele Registry

Canonical Allele Identifier: PA2830272235

Gene: ADAMTS13 HGNC NCBI

ClinVar RCV:

RCV002119552

RCV003138076

RCV003235673

ClinVar Variation:

1590075

HGVS (amino-acid)	Matching Registered Transcripts
NP_620595.1:p.Gly951Arg	CA200940058 NM_139026.6:c.2851G>A CA375406064 NM_139026.6:c.2851G>C