Canonical Allele Identifier: PA2830271824
Gene: ADAMTS13 HGNC NCBI

Linked Data

ClinVar Variation Id: 68823
ClinVar RCV Id: RCV000059775 RCV000516791 RCV003894915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620595.1:p.Arg193Trp
CA220047
NM_139026.6:c.577C>T