Canonical Allele Identifier: PA916071838
Gene: ADAMTS13 HGNC NCBI

Linked Data

ClinVar Variation Id: 632074
ClinVar RCV Id: RCV000778929 RCV001507763 RCV003994114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620596.2:p.Asp187His
CA200922204
NM_139027.6:c.559G>C