Canonical Allele Identifier: PA2830272213
Gene: ADAMTS13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2139046
ClinVar RCV Id: RCV003066493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620595.1:p.Pro921Ser
CA200939153
NM_139026.6:c.2761C>T