Canonical Allele Identifier: PA916071816
Gene: ADAMTS13 HGNC NCBI

Linked Data

ClinVar Variation Id: 68812
ClinVar RCV Id: RCV000059764 RCV000778160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620596.2:p.Val88Met
CA220013
NM_139027.6:c.262G>A